Gerstmann-Straussler-Scheinker disease with mutation at codon 102 and methionine at codon 129 of PRNP in previously unreported patients-Reference-Cited by-同舟云学术

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Gerstmann-Straussler-Scheinker disease with mutation at codon 102 and methionine at codon 129 of PRNP in previously unreported patients

Published:1995-06-01 Issue:6 Volume:45 Page:1127-1134
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Young K.,Jones C. K.,Piccardo P.,Lazzarini A.,Golbe L. I.,Zimmerman T. R.,Dickson D. W.,McLachlan D. C.,George-Hyslop P. St.,Lennox A.,Perlman S.,Vinters H. V.,Hodes M. E.,Dlouhy S.,Ghetti B.

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 Proteinleri ve Etki Mekanizmaları;Doğu Fen Bilimleri Dergisi;2023-12-17

2. Case report: A Chinese patient with spinocerebellar ataxia finally confirmed as Gerstmann-Sträussler-Scheinker syndrome with P102L mutation;Frontiers in Neurology;2023-08-03

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

4. Application of yeast to studying amyloid and prion diseases;Advances in Genetics;2020

5. Familial Prion Disease: First Indian Kindred with Gerstmann–Sträussler–Scheinker Syndrome;Neurology India;2020

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