Mutation of thePRNP gene at codon 211 in familial Creutzfeldt-Jakob disease
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference24 articles.
1. Familial Prion Disease Mutation Alters the Secondary Structure of Recombinant Mouse Prion Protein: Implications for the Mechanism of Prion Formation
2. Prion Protein and the Transmissible Spongiform Encephalopathy Diseases
3. High incidence of Creutzfeldt-Jakob disease in rural Calabria, Italy
4. Creutzfeldt-Jacob disease associated with the PRNP codon 200LYS mutation: An analysis of 45 families
5. Fatal Familial Insomnia and Familial Creutzfeldt-Jakob Disease: Disease Phenotype Determined by a DNA Polymorphism
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1. Characterization of mutations in PRNP (prion) gene and their possible roles in neurodegenerative diseases;Neuropsychiatric Disease and Treatment;2018-08
2. Prion disease;Neurogenetics, Part II;2018
3. Genetic Creutzfeldt–Jakob disease;Human Prion Diseases;2018
4. Genetic PrP Prion Diseases;Cold Spring Harbor Perspectives in Biology;2017-08-04
5. Genetic prion disease: Experience of a rapidly progressive dementia center in the United States and a review of the literature;American Journal of Medical Genetics Part B: Neuropsychiatric Genetics;2016-12-12
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