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
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
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
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
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