NR AEKD
AU Gambetti,P.
TI Fatal familial insomnia and familial Creutzfeldt-Jakob disease: a tale of two diseases with the same genetic mutation.
QU Current Topics in Microbiology and Immunology 1996; 207: 19-25
PT journal article; review; review, tutorial
ZR 17
MH Creutzfeldt-Jakob Syndrome/*genetics/mortality; Genetic Heterogeneity; Human; Mutation; Phenotype; Prion Diseases/*genetics/mortality/physiopathology; Sleep Initiation and Maintenance Disorders/etiology/*genetics/mortality; Support, Non-U.S. Gov't; Support, U.S. Gov't, P.H.S.
AD Division of Neuropathology, Case Western Reserve University, Cleveland, OH 44106, USA
SP englisch
PO Deutschland
OR Prion-Krankheiten G