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pro vyhledávání: '"Anja Vossenkaul"'
Publikováno v:
Cells, Vol 12, Iss 18, p 2314 (2023)
A number of hereditary ataxias are caused by inborn errors of metabolism (IEM), most of which are highly heterogeneous in their clinical presentation. Prompt diagnosis is important because disease-specific therapies may be available. In this review,
Externí odkaz:
https://doaj.org/article/3f9a4295f9d444cfbddf8d2bd1a9d8f7