The ATXN2 9 bp duplication in SCA3: clarifying evidence and correcting misinterpretations

Jose Miguel Laffita-Mesa1,2, Martin Paucar3, Per Svenningsson3

  • 1Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden. jose.laffita@ki.se.

Summary

The ATXN2 9-bp duplication may modify spinocerebellar ataxia type 3 (SCA3) onset, particularly with intermediate CAG repeats. This genetic interaction, supported by DNA, RNA, and protein evidence, highlights ATXN2 variants as crucial SCA3 modifiers.

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