No correlation between clinical heterogeneity and codon 129 polymorphism of the prion protein gene (PRNP) in Gerstmann-Straussler-Scheinker Syndrome (GSS) with PRNP codon 102 mutation-Reference-Cited by-同舟云学术

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No correlation between clinical heterogeneity and codon 129 polymorphism of the prion protein gene (PRNP) in Gerstmann-Straussler-Scheinker Syndrome (GSS) with PRNP codon 102 mutation

Published:1994-01 Issue: Volume:15 Page:S156
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Barbanti P.,Fabbrini G.,Salvatore M.,Petraroli R.,Pocchiari M.,Macchi G.,Lenzi G.L.

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Neurology (clinical),Aging,General Neuroscience

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Chapter 5 Human Prion Diseases;Genetic Aberrancies and Neurodegenerative Disorders;1999

2. Prion protein hereditary amyloidosis: parenchymal and vascular;Seminars in Virology;1996-06

3. Prion Protein Amyloidosis;Brain Pathology;1996-04

4. Gerstmann-Sträussler-Scheinker Disease (PRNP P102L): Amyloid Deposits Are Best Recognized by Antibodies Directed to Epitopes in PrP Region 90-165;Journal of Neuropathology and Experimental Neurology;1995-11

5. Gerstmann-Sträussler-Scheinker Disease and the Indiana Kindred;Brain Pathology;1995-01

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