Abnormal Properties of Prion Protein with Insertional Mutations in Different Cell Types
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference40 articles.
1. Prions and related neurological diseases
2. Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene.
3. INHERITED PRION DISEASE WITH 144 BASE PAIR GENE INSERTION: 1. GENEALOGICAL AND MOLECULAR STUDIES
4. An in-frame insertion in the prion protein gene in familial Creutzfeldt-Jakob disease
5. A new (two‐repeat) octapeptide coding insert mutation in Creutzfeldt‐Jakob disease
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