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Agrypnia excitata and obstructive apnea in a patient with fatal familial insomnia from China: A case report
RATIONALE: Fatal familial insomnia (FFI) linked to a D178N/129M haplotype mutation in the PRNP gene is the most common genetic prion disease in the Han Chinese population. Here, we describe a Han Chinese patient with FFI who exhibited agrypnia excitata and obstructive apnea. PATIENT CONCERNS: A 46-y...
Autores principales: | Sun, Congcong, Xia, Wen, Liu, Ying, Jia, Guoyong, Wang, Cuilan, Yan, Chuanzhu, Li, Yi |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5728880/ https://www.ncbi.nlm.nih.gov/pubmed/29245265 http://dx.doi.org/10.1097/MD.0000000000008951 |
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