A missense mutation at codon 105 with codon 129 polymorphism of the prison protein gene in a new variant of Gerstmann-Strassler-Scheinker disease-Reference-Cited by-同舟云学术

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A missense mutation at codon 105 with codon 129 polymorphism of the prison protein gene in a new variant of Gerstmann-Strassler-Scheinker disease

Published:1993-12-01 Issue:12 Volume:43 Page:2723-2723
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Yamada M.,Itoh Y.,Fujigasaki H.,Naruse S.,Kaneko K.,Kitamoto T.,Tateishi J.,Otomo E.,Hayakawa M.,Tanaka J.,Matsushita M.,Miyatake T.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 43 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. Prion Diseases;Emerging Human Viral Diseases, Volume II;2024

2. Genetics of Prion Disease;Prions and Diseases;2023

3. Methionine homozygosity for PRNP polymorphism and susceptibility to human prion diseases;Journal of Neurology, Neurosurgery & Psychiatry;2022-04-06

4. Clinical and Laboratory Features of Three Rare Chinese V210I gCJD Patients;Pathogens;2020-09-28

5. An autopsy report of three kindred in a Gerstmann-Sträussler-Scheinker disease P105L family with a special reference to prion protein, tau, and beta-amyloid;Brain and Behavior;2018-09-21

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