A Chinese Creutzfeldt-Jakob disease patient with E196K mutation in PRNP

Genetic Creutzfeldt-Jakob disease (gCJD) is caused by a range of mutations in the prion protein gene (PRNP) and account for approximately 10–15% of overall human prion diseases worldwide. They are different with disease onset, disease duration, clinical signs and diagnostic findings. Here we reporte...

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Detalhes bibliográficos
Main Authors: Shi, Qi, Chen, Cao, Song, Xiao-Nan, Gao, Chen, Tian, Chan, Zhou, Wei, Song, Xu-Hua, Yao, Lai-Shun, Han, Jun, Dong, Xiao-Ping
Formato: Artigo
Idioma:Inglês
Publicado em: Landes Bioscience 2011
Assuntos:
Technical Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3166511/
https://ncbi.nlm.nih.gov/pubmed/21597335
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/pri.5.2.15846
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