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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| Auteurs principaux: | , , , , , |
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| Format: | Artigo |
| Langue: | Russo |
| Publié: |
Open Systems Publication
2024-10-01
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| Collection: | Лечащий Врач |
| Sujets: | |
| Accès en ligne: | https://journal.lvrach.ru/jour/article/view/1292 |
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