Fatal familial insomnia, associated with PRNP mutation (clinical case)

Background. Prion diseases or transmissible spongiform encephalopathies are a group of neurodegenerative disorders characterized by rapidly progressive dementia and movement disorders. Prion diseases can be acquired, sporadic, genetic (inherited), and are characterized by the accumulation and aggreg...

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發表在:	Лечащий Врач
Main Authors:	T. V. Kozhanova, S. S. Zhylina, T. I. Meshcheryakova, E. S. Bolshakova, K. V. Osipova, N. N. Zavadenko
格式:	Article
語言:	俄语
出版:	Open Systems Publication 2024-10-01
主題:	fatal familial insomnia prnp gene whole exome sequencing
在線閱讀:	https://journal.lvrach.ru/jour/article/view/1292