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pro vyhledávání: '"E. Y. Fedotova"'
Publikováno v:
Неврология, нейропсихиатрия, психосоматика, Vol 14, Iss 6, Pp 63-66 (2022)
The article presents a description of the family case of rare hereditary prion disease – Gerstmann–Sträussler–Scheinker syndrome with a verified p.P102L mutation in the PRNP gene. The clinical picture was represented by progressive cerebellar
Externí odkaz:
https://doaj.org/article/36a9b0649a9e4a4e8eb680dda1058c15
