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Human Molecular Genetics|March 19, 2026
Association of rare apolipoprotein E ε4 homozygosity with an earlier age at onset in spinocerebellar ataxia type 3Charlotte Clara Meyer, Eduardo Preusser de Mattos, Rahel Maria Burger, et al.Acta Neuropathologica|August 1, 2024
The parkin V380L variant is a genetic modifier of Machado-Joseph disease with impact on mitophagyJonasz J Weber, Leah Czisch, Priscila Pereira Sena, et al.Pageof 3