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Prion Volume 16, 2022 - Issue 1
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Case Report

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

Yuheng Shana Medical School of Chinese PLA, Beijing, P.R. China;b Department of Neurology, The First Medical Centre, Chinese PLA General Hospital, Beijing, P.R. China;c Department of Neurology, Characteristic Medical Centre of People’s Armed Police Force, Tianjin, P.R. ChinaView further author information
,
Jiatang Zhangb Department of Neurology, The First Medical Centre, Chinese PLA General Hospital, Beijing, P.R. ChinaCorrespondence[email protected]
ORCID Iconhttps://orcid.org/0000-0002-9714-0944View further author information
ORCID Icon,
Yuying Cena Medical School of Chinese PLA, Beijing, P.R. China;b Department of Neurology, The First Medical Centre, Chinese PLA General Hospital, Beijing, P.R. ChinaView further author information
,
Xiaojiao Xua Medical School of Chinese PLA, Beijing, P.R. China;b Department of Neurology, The First Medical Centre, Chinese PLA General Hospital, Beijing, P.R. ChinaView further author information
,
Ruishu Tana Medical School of Chinese PLA, Beijing, P.R. China;b Department of Neurology, The First Medical Centre, Chinese PLA General Hospital, Beijing, P.R. ChinaView further author information
,
Jiahua Zhaoa Medical School of Chinese PLA, Beijing, P.R. China;b Department of Neurology, The First Medical Centre, Chinese PLA General Hospital, Beijing, P.R. ChinaView further author information
&
Shengyuan Yub Department of Neurology, The First Medical Centre, Chinese PLA General Hospital, Beijing, P.R. ChinaView further author information
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Pages 14-18 | Received 27 Nov 2021, Accepted 14 Jan 2022, Published online: 07 Feb 2022

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