Spontaneous mutations in the prion protein gene causing transmissible spongiform encephalopathy

Author:

Dagvadorj Ayush,Petersen Robert B.,Lee Hee Suk,Cervenakova Larisa,Shatunov Alexey,Budka Herbert,Brown Paul,Gambetti Pierluigi,Goldfarb Lev G.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference14 articles.

1. Transmissible human spongiform encephalopathy (infectious cerebral amyloidosis): Creutzfeldt-Jakob disease, Gerstmann-Sträussler-Scheinker Syndrome, and Kuru. In: ed. Neurodegenerative diseases. Philadelphia: WB Saunders, 1994: 839-876.

2. et al. Inherited prion diseases. In: ed. Prion biology and diseases. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press, 1999: 509-583.

3. Fatal Familial Insomnia, a Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene

4. Mutation in codon 200 of scrapie amyloid protein gene in two clusters of Creutzfeldt-Jakob disease in Slovakia

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