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pro vyhledávání: '"Martina Troisi"'
Autor:
Valentina Naef, Maria Lieto, Sara Satolli, Rosa De Micco, Martina Troisi, Rosa Pasquariello, Stefano Doccini, Flavia Privitera, Alessandro Filla, Alessandro Tessitore, Filippo Maria Santorelli
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 11, Iss 7, Pp 1879-1886 (2024)
Abstract Objective Biallelic mutations in PRDX3 have been linked to autosomal recessive spinocerebellar ataxia type 32. In this study, which aims to contribute to the growing body of knowledge on this rare disease, we identified two unrelated patient
Externí odkaz:
https://doaj.org/article/a437eab8187e40a1ba297e899e00ac27
