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Genetic Creutzfeldt-Jakob disease shows fatal family insomnia phenotype
We report a case of genetic Creutzfeldt-Jakob disease (gCJD), which has a clinical phenotype that is highly similar to Fatal Family Insomnia (FFI) and has a triad of Wernicke-Korsakoff syndrome (WKs) at the developmental stage of the disease. The 51-year-old male complained of sleep disorder and imb...
Autores principales: | Chen, Bin, Zhang, Shan, Xiao, Ying, Wu, yingman, Tang, Weiting, Yan, Limin, Zhang, Zhengxue, Qin, Shengquan, Dai, Mingming, You, Yong |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8425754/ https://www.ncbi.nlm.nih.gov/pubmed/34486485 http://dx.doi.org/10.1080/19336896.2021.1968291 |
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