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Prion Volume 13, 2019 - Issue 1
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Rare genetic Creutzfeldt-Jakob disease with E196A mutation: a case report

Yanyuan DaiDepartment of Neurology, Neuroscience Center, The First Hospital of Jilin University, Jilin University, Changchun, ChinaView further author information
,
Yue LangDepartment of Neurology, Neuroscience Center, The First Hospital of Jilin University, Jilin University, Changchun, ChinaView further author information
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Mingxuan DingDepartment of Neurology, Neuroscience Center, The First Hospital of Jilin University, Jilin University, Changchun, ChinaView further author information
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Baizhuo ZhangDepartment of Neurology, Neuroscience Center, The First Hospital of Jilin University, Jilin University, Changchun, ChinaView further author information
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Xiaoou HanDepartment of Neurology, Neuroscience Center, The First Hospital of Jilin University, Jilin University, Changchun, ChinaView further author information
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Guangyu DuanDepartment of Neurology, Neuroscience Center, The First Hospital of Jilin University, Jilin University, Changchun, ChinaView further author information
&
Li CuiDepartment of Neurology, Neuroscience Center, The First Hospital of Jilin University, Jilin University, Changchun, ChinaCorrespondence[email protected]
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Pages 132-136 | Received 05 Feb 2019, Accepted 10 Jun 2019, Published online: 25 Jun 2019

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