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The genetic Creutzfeldt-Jakob disease with E200K mutation: analysis of clinical, genetic and laboratory features of 30 Chinese patients

Genetic Creutzfeldt-Jakob disease (gCJD) with E200K mutation is one of the common subtypes of human genetic prion diseases worldwide. In this study, we systematically analyzed 30 Chinese E200K gCJD cases for their epidemiological, clinical, laboratory and genetic features. The patients came from 12...

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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Sci Rep
Egile Nagusiak: Gao, Li-Ping, Shi, Qi, Xiao, Kang, Wang, Jing, Zhou, Wei, Chen, Cao, Dong, Xiao-Ping
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Nature Publishing Group UK 2019
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC6372685/
https://ncbi.nlm.nih.gov/pubmed/30755683
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-019-38520-y
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