Evidence for a Pathogenic Role of Different Mutations at Codon 188 of PRNP-Reference-Cited by-同舟云学术

Evidence for a Pathogenic Role of Different Mutations at Codon 188 of PRNP

Published:2008-05-14 Issue:5 Volume:3 Page:e2147
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Roeber Sigrun,Grasbon-Frodl Eva-Maria,Windl Otto,Krebs Bjarne,Xiang Wei,Vollmert Caren,Illig Thomas,Schröter Andreas,Arzberger Thomas,Weber Petra,Zerr Inga,Kretzschmar Hans A.

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference42 articles.

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4. Genetic prion disease: the EUROCJD experience.;GG Kovacs;Hum Genet,2005

5. Molecular genetics of human prion diseases in Germany.;O Windl;Hum Genet,1999

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4. T188K-Familial Creutzfeldt–Jacob Disease, Predominant Among Chinese, has a Reactive Pattern in CSF RT-QuIC Different from D178N-Fatal Familial Insomnia and E200K-Familial CJD;Neuroscience Bulletin;2019-03-05

5. Clinical and neuropathological phenotype associated with the novel V189I mutation in the prion protein gene;Acta Neuropathologica Communications;2019-01-03