Analysis of 12 Chinese Patients with Proline-to-Leucine Mutation at Codon 102-Associated Gerstmann-Sträussler-Scheinker Disease

BACKGROUND AND PURPOSE: Gerstmann-Sträussler-Scheinker disease (GSS) with a proline-to-leucine mutation at codon 102 (P102L) in the PRNP gene is the most frequently reported GSS subtype worldwide. This study aimed to determine the epidemiological, clinical, genetic, and laboratory characteristics of...

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Detalles Bibliográficos
Autores principales: Wang, Jing, Xiao, Kang, Zhou, Wei, Shi, Qi, Dong, Xiao-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Neurological Association 2019
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6444146/
https://www.ncbi.nlm.nih.gov/pubmed/30877692
http://dx.doi.org/10.3988/jcn.2019.15.2.184

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6444146/
https://www.ncbi.nlm.nih.gov/pubmed/30877692
http://dx.doi.org/10.3988/jcn.2019.15.2.184

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