APTN - Dranovsky,A.; Goldfarb,L.; Gajdusek,D.C.; Goldgaber,D. - Apolipoprotein-e epsilon-4 allele does not correlate with amyloid plaques in transmissible spongiform encephalopathies - Amyloid - International Journal of Experimental and Clinical Investigation 1995 Mar; 2(1): 36-8
AFBA - Haltia,M.; Viitanen,M.; Sulkava,R.; Ala-Hurula,V.; Poyhonen,M.; Goldfarb,L.; Brown,P.; Levy,E.; Houlden,H.; Crook,R.; Goate,A.; Clark,R.; Korenblat,K.; Pandit,S.; Keller,H.D.; Lilius,L.; Liu,L.; Axelman,K.; Forsell,L.; Winblad,B.; Lannfeldt,L.; Hardy,J. - Chromosome 14-encoded Alzheimer's disease: genetic and clinicopathological description. - Annals of Neurology 1994 Sep; 36(3): 362-7
AUAO - Hardy,J.; Scholz,S.; Evans,W.; Goldfarb,L.; Singleton,A. - Prion genotypes in Central America suggest selection for the V129 allele - American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the official publication of the International Society of Psychiatric Genetics 2006 Jan 5; 141(1): 33-5
AKLG - Saunders,A.M.; Schmader,K.; Breitner,J.C.S.; Benson,M.D.; Brown,W.T.; Goldfarb,L.; Goldgaber,D.; Manwaring,M.G.; Szymanski,M.H.; McCown,N.; Dote,K.C.; Schmechel,D.E.; Strittmatter,W.J.; Pericak-Vance,M.A.; Roses,A.D. - Apolipoprotein E epsilon 4 allele distributions in late-onset Alzheimer's disease and in other amyloid-forming diseases - Lancet 1993 Sep 18; 342(8873): 710-1
ABHQ - Bertoni,J.M.; Brown,P.; Goldfarb,L.G.; Rubenstein,R.; Gajdusek,D.C. - Familial Creutzfeldt-Jakob disease (codon 200 mutation) with supranuclear palsy - JAMA. Journal of the American Medical Association 1992 Nov 4; 268(17): 2413-5
ABUP - Brown,P.; Cervenakova,L.; McShane,L.; Goldfarb,L.G.; Bishop,K.; Bastian,F.O.; Kirkpatrick,J.; Piccardo,P.; Ghetti,B.; Gajdusek,D.C. - Creutzfeldt-Jakob disease in a husband and wife - Neurology 1998 Mar; 50(3): 684-8
AOEE - Brown,P.; Chapman,J.C.; Cervenakova,L.; Goldfarb,L.G.; Korczyn,A.D. - Cell-free expression of the prnp gene containing a large insert associated with Creutzfeldt-Jakob-disease - Neurology 1996; 46(N2): S01.003
ABUV - Brown,P.; Cervenakova,L.; Boellaard,J.W.; Stavrou,D.; Goldfarb,L.G.; Gajdusek,D.C. - Identification of a PRNP gene mutation in Jakob's original Creutzfeldt-Jakob disease family - Lancet 1994 Jul 9; 344(8915): 130-1
ABUW - Brown,P.; Gibbs,C.J.Jr.; Rodgers-Johnson,P.; Asher,D.M.; Sulima,M.P.; Bacote,A.E.; Goldfarb,L.G.; Gajdusek,D.C. - Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease. - Annals of Neurology 1994 May; 35(5): 513-29
ABUY - Brown,P.; Cervenakova,L.; Goldfarb,L.G.; McCombie,W.R.; Rubenstein,R.; Will,R.G.; Pocchiari,M.; Martinez-Lage,J.F.; Scalici,C.; Masullo,C.; Graupera,G.; Ligan,J.; Gajdusek,D.C. - Iatrogenic Creutzfeldt-Jakob Disease: An example of the interplay between ancient genes and modern medicine - Neurology 1994 Feb; 44(2): 291-3
ABUZ - Brown,P.; Cervenakova,L.; Goldfarb,L.G.; Gajdusek,D.C.; Haverkamp,A.; Haverkamp,C.; Horwitz,J.; Creacy,S.D.; Bever,R.A.; Wexler,P.; Sujansky,E.; Bjork,R.J. - Molecular genetic testing of a fetus at risk of Gerstmann-Sträussler-Scheinker syndrome - Lancet 1994 Jan 15; 343(8890): 181-2
ABVB - Brown,P.; Kaur,P.; Sulima,M.P.; Goldfarb,L.G.; Gibbs,C.J.Jr.; Gajdusek,D.C. - Real and imagined clinicopathological limits of "prion dementia" - Lancet 1993 Jan 16; 341(8838): 127-9
ABVD - Brown,P.; Galvez,S.; Goldfarb,L.G.; Nieto,A.; Cartier,L.R.; Gibbs,C.J.Jr.; Gajdusek,D.C. - Familial Creutzfeldt-Jakob disease in Chile is associated with the codon 200 mutation of the PRNP amyloid precursor gene on chromosome 20 - Journal of the Neurological Sciences 1992 Oct; 112(1-2): 65-7
ABVF - Brown,P.; Goldfarb,L.G.; Kovanen,J.; Haltia,M.; Cathala,F.; Sulima,M.; Gibbs,C.J.Jr.; Gajdusek,D.C. - Phenotypic characteristics of familial Creutzfeldt-Jakob disease associated with the codon 178Asn PRNP mutation - Annals of Neurology 1992 Mar; 31(3): 282-5
ABVG - Brown,P.; Goldfarb,L.G.; McCombie,W.R.; Nieto,A.; Squillacote,D.; Sheremata,W.; Little,B.W.; Godec,M.S.; Gibbs,C.J.Jr.; Gajdusek,D.C. - Atypical Creutzfeldt-Jakob disease in an American family with an insert mutation in the PRNP amyloid precursor gene - Neurology 1992 Feb; 42(2): 422-7
ABVI - Brown,P.; Goldfarb,L.G.; Cathala,F.; Vrbovska,A.; Sulima,M.; Nieto,A.; Gibbs,C.J.Jr.; Gajdusek,D.C. - The molecular genetics of familial Creutzfeldt-Jakob disease in France - Journal of the Neurological Sciences 1991 Oct; 105(2): 240-6
ABVJ - Brown,P.; Goldfarb,L.G.; Gibbs,C.J.Jr.; Gajdusek,D.C. - The phenotypic expression of different mutations in transmissible familial Creutzfeldt-Jakob disease - European Journal of Epidemiology 1991 Sep; 7(5): 469-76
ABVK - Brown,P.; Goldfarb,L.G.; Gajdusek,D.C. - The new biology of spongiform encephalopathy: infectious amyloidoses with a genetic twist. - Lancet 1991 Apr 27; 337(8748): 1019-22
ABVL - Brown,P.; Goldfarb,L.G.; Brown,W.T.; Goldgaber,D.; Rubenstein,R.; Kascsak,R.J.; Guiroy,D.C.; Piccardo,P.; Boellaard,J.W.; Gajdusek,D.C. - Clinical and molecular genetic study of a large German kindred with Gerstmann-Sträussler-Scheinker syndrome - Neurology 1991 Mar; 41(3): 375-9
ACBI - Butefisch,C.M.; Gambetti,P.; Cervenakova,L.; Park,K.Y.; Hallett,M.; Goldfarb,L.G. - Inherited prion encephalopathy associated with the novel PRNP H187R mutation: a clinical study. - Neurology 2000 Aug 22; 55(4): 517-22
ACEG - Camenga,D.L.; Goldfarb,L.G.; Bierke-Nelson,D.; Neff,K. - Familial Creutzfeldt-Jakob disease - Slow Infections of the Central Nervous System (Ed. Bjornsson, J.; Carp, R.I.; Love, A.; Wisniewski, H.M.) 1994 Jun 6; 724: 361-2
ACLG - Cervenakova,L.; Buetefisch,C.; Lee,H.S.; Taller,I.; Stone,G.; Gibbs,C.J.Jr.; Brown,P.; Hallett,M.; Goldfarb,L.G. - Novel PRNP sequence variant associated with familial encephalopathy - American Journal of Medical Genetics 1999 Dec 15; 88(6): 653-6
ACLH - Cervenakova,L.; Goldfarb,L.G.; Garruto,R.; Lee,H.S.; Gajdusek,D.C.; Brown,P. - Phenotype-genotype studies in kuru: implications for new variant Creutzfeldt-Jakob disease. - Proceedings of the National Academy of Sciences of the United States of America 1998 Oct 27; 95(22): 13239-41
ACLK - Cervenakova,L.; Sivakumar,K.; Nagle,J.; Dalakas,M.C.; Goldfarb,L.G. - Is hereditary inclusion body myopathy a "familial prion disease" ? - Annals of Neurology 1996 Jul; 40(1): 128
APOC - Cervenakova,L.; Goldfarb,L.G.; Brown,P.; Kenney,K.; Cochran,E.J.; Bennett,D.A.; Roos,R.; Gajdusek,D.C. - 3 new prnp genotypes associated with familial Creutzfeldt-Jakob-disease - American Journal of Human Genetics 1995; 57(N4): 1207
APOD - Cervenakova,L.; Brown,P.; Goldfarb,L.G.; Nagle,J.; Pettrone,K.; Rubenstein,R.; Dubnick,M.; Gibbs,C.J.Jr.; Gajdusek,D.C. - Infectious amyloid precursor gene-sequences in primates used for experimental transmission of human spongiform encephalopathy (Correction of vol 91, pg 12159, 1994) - Proceedings of the National Academy of Sciences of the United States of America 1995 Apr 11; 92(8): 3631
ACLJ - Cervenakova,L.; Brown,P.; Goldfarb,L.G.; Nagle,J.; Pettrone,K.; Rubenstein,R.; Dubnick,M.; Gibbs,C.J.Jr.; Gajdusek,D.C. - Infectious amyloid precursor gene sequences in primates used for experimental transmission of human spongiform encephalopathy - Proceedings of the National Academy of Sciences of the United States of America 1994 Dec 6; 91(25): 12159-62
ACMQ - Chapman,J.C.; Cervenakova,L.; Petersen,R.B.; Lee,H.S.; Estupinan,J.; Richardson,S.; Vnencak-Jones,C.L.; Gajdusek,D.C.; Korczyn,A.D.; Brown,P.; Goldfarb,L.G. - APOE in non-Alzheimer amyloidoses: transmissible spongiform encephalopathies. - Neurology 1998 Aug; 51(2): 548-53
ACMR - Chapman,J.C.; Arlazoroff,A.; Goldfarb,L.G.; Cervenakova,L.; Neufeld,M.Y.; Werber,E.; Herbert,M.; Brown,P.; Gajdusek,D.C.; Korczyn,A.D. - Fatal insomnia in a case of familial Creutzfeldt-Jakob disease with the codon 200(Lys) mutation - Neurology 1996 Mar; 46(3): 758-61
ACMT - Chapman,J.C.; Brown,P.; Goldfarb,L.G.; Arlazoroff,A.; Gajdusek,D.C.; Korczyn,A.D. - Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutation - Journal of Neurology, Neurosurgery and Psychiatry 1993 Oct; 56(10): 1109-12
ACMU - Chapman,J.C.; Brown,P.; Rabey,J.M.; Goldfarb,L.G.; Inzelberg,R.; Gibbs,C.J.Jr.; Gajdusek,D.C.; Korczyn,A.D. - Transmission of spongiform encephalopathy from a familial Creutzfeldt-Jakob disease patient of Jewish Libyan origin carrying the PRNP codon 200 mutation - Neurology 1992 Jun; 42(6): 1249-50
ACRU - Cochran,E.J.; Bennett,D.A.; Cervenakova,L.; Kenney,K.; Bernard,B.; Foster,N.L.; Benson,D.F.; Goldfarb,L.G.; Brown,P. - Familial Creutzfeldt-Jakob disease with a five-repeat octapeptide insert mutation - Neurology 1996 Sep; 47(3): 727-33
AUZA - Colucci,M.; Moleres,F.J.; Xie,Z.L.; Ray-Chaudhury,A.; Gutti,S.; Butefisch,C.M.; Cervenakova,L.; Wang,W.; Goldfarb,L.G.; Kong,Q.; Ghetti,B.; Chen,S.G.; Gambetti,P. - Gerstmann-Sträussler-Scheinker: a new phenotype with 'curly' PrP deposits. - Journal of Neuropathology and Experimental Neurology 2006 Jul; 65(7): 642-51
ACZX - Dagvadorj,A.; Petersen,R.B.; Lee,H.S.; Cervenakova,L.; Shatunov,A.; Budka,H.; Brown,P.; Gambetti,P.; Goldfarb,L.G. - Spontaneous mutations in the prion protein gene causing transmissible spongiform encephalopathy - Annals of Neurology 2002 Sep; 52(3): 355-9
APWQ - El Hachimi,K.H.; Cervenakova,L.; Brown,P.; Goldfarb,L.G.; Rubenstein,R.; Gajdusek,D.C.; Foncin,J.F. - Mixed features of Alzheimer-disease and Creutzfeldt-Jakob- disease in a family with a presenilin-1 mutation in chromosome-14 - Amyloid - International Journal of Experimental and Clinical Investigation 1996; 3(N4): 223-33
ARHG - Goldfarb,L.G.; Cervenakova,L.; Gajdusek,D.C. - Genetic studies in relation to kuru: an overview. - Current Molecular Medicine 2004 Jun; 4(4): 375-84
AEQR - Goldfarb,L.G. - Kuru: the old epidemic in a new mirror. - Microbes and Infection 2002 Jul; 4(8): 875-82
AEQS - Goldfarb,L.G. - Genetics and infectious disease: convergence at the prion. - Epidemiology 2002 Jul; 13(4): 379-81
AQED - Goldfarb,L.G.; Chapman,J.C.; Brown,P.; Cervenakova,L.; Gajdusek,D.C.; Korczyn,A.D. - Apolipoprotein-e genotype in human spongiform encephalopathies - Neurology 1996; 46(N2): 2064
AEQT - Goldfarb,L.G.; Brown,P. - The transmissible spongiform encephalopathies - Annual Review of Medicine 1995; 46: 57-65
AEQU - Goldfarb,L.G.; Brown,P.; Cervenakova,L.; Gajdusek,D.C. - Molecular genetic studies of Creutzfeldt-Jakob disease - Molecular Neurobiology 1994 Apr-Jun; 8(2-3): 89-97
AEQV - Goldfarb,L.G.; Brown,P.; Cervenakova,L.; Gajdusek,D.C. - Genetic analysis of Creutzfeldt-Jakob disease and related disorders - Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences 1994 Mar 29; 343(1306): 379-84
AEQW - Goldfarb,L.G.; Brown,P.; Little,B.W.; Cervenakova,L.; Kenney,K.; Gibbs,C.J.Jr.; Gajdusek,D.C. - A new (two-repeat) octapeptide coding insert mutation in Creutzfeldt-Jakob disease - Neurology 1993 Nov; 43(11): 2392-4
AEQX - Goldfarb,L.G.; Brown,P.; Haltia,M.; Ghiso,J.; Frangione,B.; Gajdusek,D.C. - Synthetic peptides corresponding to different mutated regions of the amyloid gene in familial Creutzfeldt-Jakob disease show enhanced in vitro formation of morphologically different amyloid fibrils - Proceedings of the National Academy of Sciences of the United States of America 1993 May 15; 90(10): 4451-4
AEQY - Goldfarb,L.G.; Petersen,R.B.; Tabaton,M.; Brown,P.; LeBlanc,A.C.; Montagna,P.; Cortelli,P.; Julien,J.; Vital,C.; Pendelbury,W.W.; Haltia,M.; Willis,P.R.; Hauw,J.J.; McKeever,P.E.; Monari,L.; Schrank,B.; Swergold,G.D.; Autilio-Gambetti,L.; Gajdusek,D.C.; Lugaresi,E.; Gambetti,P. - Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism. - Science 1992 Oct 30; 258(5083): 806-8
AEQZ - Goldfarb,L.G.; Brown,P.; Vrbovska,A.; Baron,H.; McCombie,W.R.; Cathala,F.; Gibbs,C.J.Jr.; Gajdusek,D.C. - An insert mutation in the chromosome 20 amyloid precursor gene in a Gerstmann-Sträussler-Scheinker family - Journal of the Neurological Sciences 1992 Sep; 111(2): 189-94
AERA - Goldfarb,L.G.; Brown,P.; Haltia,M.; Cathala,F.; McCombie,W.R.; Kovanen,J.; Cervenakova,L.; Goldin,L.; Nieto,A.; Godec,M.S.; et al. - Creutzfeldt-Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European origin - Annals of Neurology 1992 Mar; 31(3): 274-81
AERB - Goldfarb,L.G.; Brown,P.; McCombie,W.R.; Goldgaber,D.; Swergold,G.D.; Wills,P.R.; Cervenakova,L.; Baron,H.; Gibbs,C.J.Jr.; Gajdusek,D.C. - Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene - Proceedings of the National Academy of Sciences of the United States of America 1991 Dec 1; 88(23): 10926-30
AERC - Goldfarb,L.G.; Brown,P.; Mitrova,E.; Cervenakova,L.; Goldin,L.; Korczyn,A.D.; Chapman,J.C.; Galvez,S.; Cartier,L.R.; Rubenstein,R.; Gajdusek,D.C. - Creutzfeldt-Jakob disease associated with the PRNP codon 200Lys mutation: an analysis of 45 families. - European Journal of Epidemiology 1991 Sep; 7(5): 477-86
AERD - Goldfarb,L.G.; Haltia,M.; Brown,P.; Nieto,A.; Kovanen,J.; McCombie,W.R.; Trapp,S.; Gajdusek,D.C. - New mutation in scrapie amyloid precursor gene (at codon 178) in Finnish Creutzfeldt-Jakob kindred - Lancet 1991 Feb 16; 337(8738): 425
AERE - Goldfarb,L.G.; Korczyn,A.D.; Brown,P.; Chapman,J.C.; Gajdusek,D.C. - Mutation in codon 200 of scrapie amyloid precursor gene linked to Creutzfeldt-Jakob disease in Sephardic Jews of Libyan and non-Libyan origin - Lancet 1990 Sep 8; 336(8715): 637-8
AERF - Goldfarb,L.G.; Mitrova,E.; Brown,P.; Toh,B.K.; Gajdusek,D.C. - Mutation in codon 200 of scrapie amyloid protein gene in two clusters of Creutzfeldt-Jakob disease in Slovakia - Lancet 1990 Aug 25; 336(8713): 514-5
AERG - Goldfarb,L.G.; Brown,P.; Goldgaber,D.; Garruto,R.M.; Yanagihara,R.; Asher,D.M.; Gajdusek,D.C. - Identical mutation in unrelated patients with Creutzfeldt-Jakob disease - Lancet 1990 Jul 21; 336(8708): 174-5
AERH - Goldfarb,L.G.; Brown,P.; Goldgaber,D.; Asher,D.M.; Rubenstein,R.; Brown,W.T.; Piccardo,P.; Kascsak,R.J.; Boellaard,J.W.; Gajdusek,D.C. - Creutzfeldt-Jakob disease and kuru patients lack a mutation consistently found in the Gerstmann-Sträussler-Scheinker syndrome - Experimental Neurology 1990 Jun; 108(3): 247-50
AERJ - Goldgaber,D.; Goldfarb,L.G.; Brown,P.; Asher,D.M.; Brown,W.T.; Lin,S.; Teener,J.W.; Feinstone,S.M.; Rubenstein,R.; Kascsak,R.J.; Boellaard,J.W.; Gajdusek,D.C. - Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndrome - Experimental Neurology 1989 Nov; 106(2): 204-6
AFBC - Haltia,M.; Kovanen,J.; Goldfarb,L.G.; Brown,P.; Gajdusek,D.C. - Familial Creutzfeldt-Jakob disease in Finland: epidemiological, clinical, pathological and molecular genetic studies. - European Journal of Epidemiology 1991 Sep; 7(5): 494-500
AGRW - Korczyn,A.D.; Chapman,J.C.; Goldfarb,L.G.; Brown,P.; Gajdusek,D.C. - A mutation in the prion protein gene in Creutzfeldt-Jakob disease in Jewish patients of Libyan, Greek, and Tunisian origin - Annals of the New York Academy of Sciences 1991; 640: 171-6
AHDK - Lee,H.S.; Brown,P.; Cervenakova,L.; Garruto,R.M.; Alpers,M.P.; Gajdusek,D.C.; Goldfarb,L.G. - Increased susceptibility to Kuru of carriers of the PRNP 129 methionine/methionine genotype - Journal of Infectious Diseases 2001 Jan 15; 183(2): 192-196
AHDL - Lee,H.S.; Sambuughin,N.; Cervenakova,L.; Chapman,J.C.; Pocchiari,M.; Litvak,S.; Qi,H.Y.; Budka,H.; del Ser,T.; Furukawa,H.; Brown,P.; Gajdusek,D.C.; Long,J.C.; Korczyn,A.D.; Goldfarb,L.G. - Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease - American Journal of Human Genetics 1999 Apr; 64(4): 1063-70
AHST - Majtenyi,C.; Brown,P.; Cervenakova,L.; Goldfarb,L.G.; Tateishi,J. - A three-sister sibship of Gerstmann-Sträussler-Scheinker disease with a CJD phenotype - Neurology 2000 Jun 13; 54(11): 2133-7
AIND - Monari,L.; Chen,S.G.; Brown,P.; Parchi,P.; Petersen,R.B.; Mikol,J.; Gray,F.; Cortelli,P.; Montagna,P.; Ghetti,B.; Goldfarb,L.G.; Gajdusek,D.C.; Lugaresi,E.; Gambetti,P.; Autilio-Gambetti,L. - Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism. - Proceedings of the National Academy of Sciences of the United States of America 1994 Mar 29; 91(7): 2839-42
AINW - Mora,C.A.; Garruto,R.M.; Brown,P.; Guiroy,D.; Morgan,O.S.; Rodgers-Johnson,P.; Ceroni,M.; Yanagihara,R.; Goldfarb,L.G.; Gibbs,C.J.Jr.; et al. - Seroprevalence of antibodies to HTLV-I in patients with chronic neurological disorders other than tropical spastic paraparesis - Annals of Neurology 1988; 23 Suppl: S192-5
AIWM - Nieto,A.; Goldfarb,L.G.; Brown,P.; McCombie,W.R.; Trapp,S.; Asher,D.M.; Gajdusek,D.C. - Codon 178 mutation in ethnically diverse Creutzfeldt-Jakob disease families - Lancet 1991 Mar 9; 337(8741): 622-3
AJKH - Petersen,R.B.; Goldfarb,L.G.; Tabaton,M.; Brown,P.; Monari,L.; Cortelli,P.; Montagna,P.; Autilio-Gambetti,L.; Gajdusek,D.C.; Lugaresi,E.; Gambetti,P. - A novel mechanism of phenotypic heterogeneity demonstrated by the effect of a polymorphism on a pathogenic mutation in the PRNP (prion protein gene) - Molecular Neurobiology 1994 Apr-Jun; 8(2-3): 99-103
AJWX - Reder,A.T.; Mednick,A.S.; Brown,P.; Spire,J.P.; van Cauter,E.; Wollmann,R.L.; Cervenakova,L.; Goldfarb,L.G.; Garay,A.; Ovsiew,F.; Gajdusek,D.C.; Roos,R.P. - Clinical and genetic studies of fatal familial insomnia - Neurology 1995 Jun; 45(6): 1068-75
ARUV - Shatunov,A.; Fridman,E.A.; Pagan,F.I.; Leib,J.; Singleton,A.; Hallett,M.; Goldfarb,L.G. - Small de novo duplication in the repeat region of the TATA-box-binding protein gene manifest with a phenotype similar to variant Creutzfeldt-Jakob disease - Clinical Genetics 2004 Dec; 66(6): 496-501
ALBP - Speer,M.C.; Goldgaber,D.; Goldfarb,L.G.; Roses,A.D.; Pericak-Vance,M.A. - Support of linkage of Gerstmann-Sträussler-Scheinker syndrome to the prion protein gene on chromosome 20p12-pter - Genomics 1991 Feb; 9(2): 366-8