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pro vyhledávání: '"Javeria R. Alvi"'
Autor:
Eboni M. V. Bucknor, Errin Johnson, Stephanie Efthymiou, Javeria R. Alvi, Tipu Sultan, Henry Houlden, Reza Maroofian, Ehsan G. Karimiani, Mattéa J. Finelli, Peter L. Oliver
Publikováno v:
Antioxidants, Vol 13, Iss 6, p 685 (2024)
Loss-of-function mutations in the TLDc family of proteins cause a range of severe childhood-onset neurological disorders with common clinical features that include cerebellar neurodegeneration, ataxia and epilepsy. Of these proteins, oxidation resist
Externí odkaz:
https://doaj.org/article/d764a9d44f664403965dbb7bfe8416aa
