Creutzfeldt-Jakob disease associated with a T188K homozygous mutation in the prion protein gene: a case report and review of the literature.

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第一作者： Yuheng,Shan

第一单位： Medical School of Chinese PLA, Beijing, P.R. China.

作者： Yuheng,Shan ^[1] ; Jiatang,Zhang ^[2] ; Yuying,Cen ^[3] ; Xiaojiao,Xu ^[2] ; Ruishu,Tan ^[1] ; Jiahua,Zhao ^[2] ; Shengyuan,Yu ^[1]

作者单位： Medical School of Chinese PLA, Beijing, P.R. China. ^[1] Department of Neurology, The First Medical Centre, Chinese PLA General Hospital, Beijing, P.R. China. ^[2] Department of Neurology, Characteristic Medical Centre of People's Armed Police Force, Tianjin, P.R. China. ^[3]

关键词 Creutzfeldt–Jakob disease T188K homozygote prion protein gene

主题词克-亚综合征(Creutzfeldt-Jakob Syndrome);女(雌)性(Female);纯合子(Homozygote);人类(Humans);突变(Mutation);朊病毒(Prions)

DOI 10.1080/19336896.2022.2031719

PMID 35130121

发布时间 2022-02-28

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