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Rare genetic Creutzfeldt-Jakob disease with E196A mutation: a case report

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Pages 132-136 | Received 05 Feb 2019, Accepted 10 Jun 2019, Published online: 25 Jun 2019

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Xiping Wu, Zhao Cui, Xie Guomin, Haifeng Wang, Xiaoling Zhang, Zhiguang Li, Qi Sun & Feiteng Qi. (2020) Rare genetic E196A mutation in a patient with Creutzfeldt–Jakob disease: a case report and literature. Prion 14:1, pages 143-148.
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Articles from other publishers (4)

Yong-Kang Zhang, Jia-Rui Liu, Kang-Li Yin, Yuan Zong, Yu-Zhen Wang & Ye-Min Cao. (2023) Creutzfeldt-Jakob disease presenting as Korsakoff syndrome caused by E196A mutation in PRNP gene: A case report . World Journal of Clinical Cases 11:25, pages 5982-5987.
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James A. Mastrianni. 2023. Prions and Diseases. Prions and Diseases 375 424 .
Dan Yeong Kim, Kyu Hwan Shim, Eva Bagyinszky & Seong Soo A. An. (2022) Prion Mutations in Republic of Republic of Korea, China, and Japan. International Journal of Molecular Sciences 24:1, pages 625.
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Laura Davis, Zarina Karim & Tom Dening. (2022) Diagnostic, management and nursing challenges of less common dementias: Frontotemporal dementia, alcohol-related dementia, HIV dementia and prion diseases. British Journal of Neuroscience Nursing 18:1, pages 26-37.
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