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Short Communication

Rare E196A mutation in PRNP gene of 3 Chinese patients with Creutzfeldt-Jacob disease

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Pages 331-337 | Received 01 Feb 2016, Accepted 11 May 2016, Published online: 16 Jun 2016

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Read on this site (5)

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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Eva Bagyinszky, YoungSoon Yang, Vo Van Giau, Young Chul Youn, Seong Soo A An & SangYun Kim. (2019) Novel prion mutation (p.Tyr225Cys) in a Korean patient with atypical Creutzfeldt–Jakob disease. Clinical Interventions in Aging 14, pages 1387-1397.
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Yanyuan Dai, Yue Lang, Mingxuan Ding, Baizhuo Zhang, Xiaoou Han, Guangyu Duan & Li Cui. (2019) Rare genetic Creutzfeldt-Jakob disease with E196A mutation: a case report. Prion 13:1, pages 132-136.
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Eva Bagyinszky, Vo Van Giau, Young Chul Youn, Seong Soo A An & SangYun Kim. (2018) Characterization of mutations in PRNP (prion) gene and their possible roles in neurodegenerative diseases. Neuropsychiatric Disease and Treatment 14, pages 2067-2085.
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Qing Yang, Sihuan Zhang, Liangliang Liu, Chuzhao Lei, Xinglei Qi, Fengpeng Lin, Weidong Qu, Xingshan Qi, Jiming Liu, Rongmin Wang, Hong Chen & Xianyong Lan. (2018) The evaluation of 23-bp and 12-bp insertion/deletion within the PRNP gene and their effects on growth traits in healthy Chinese native cattle breeds. Journal of Applied Animal Research 46:1, pages 505-511.
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Articles from other publishers (8)

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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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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Yu Kong, Zhongyun Chen, Jing Zhang & Liyong Wu. (2022) Erythrocyte Indices in Creutzfeldt–Jakob Disease Predict Survival Time. Frontiers in Neurology 13.
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Qi Shi, Kang Xiao, Cao Chen, Wei Zhou, Li-Ping Gao, Yue-Zhang Wu, Yuan Wang, Chao Hu, Chen Gao & Xiao-Ping Dong. (2021) Characteristics of Chinese patients with genetic CJD who have E196A or E196K mutation in PRNP : comparative analysis of patients identified in the Chinese National CJD Surveillance System . BMJ Open 11:11, pages e054551.
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Qi Shi, Cao Chen, Kang Xiao, Wei Zhou, Li-Ping Gao, Dong-Dong Chen, Yue-Zhang Wu, Yuan Wang, Chao Hu, Chen Gao & Xiao-Ping Dong. (2021) Genetic Prion Disease: Insight from the Features and Experience of China National Surveillance for Creutzfeldt-Jakob Disease. Neuroscience Bulletin 37:11, pages 1570-1582.
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Juhwan Lee & Iksoo Chang. (2019) Structural insight into conformational change in prion protein by breakage of electrostatic network around H187 due to its protonation. Scientific Reports 9:1.
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Cao Chen, Chao Hu, Qi Shi, Wei Zhou, Kang Xiao, Yuan Wang, Lian Liu, Jia Chen, Ying Xia & Xiao-Ping Dong. (2019) Profiles of 14-3-3 and Total Tau in CSF Samples of Chinese Patients of Different Genetic Prion Diseases. Frontiers in Neuroscience 13.
Crossref
Anna Ladogana & Gabor G. Kovacs. 2018. Human Prion Diseases. Human Prion Diseases 219 242 .

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