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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.
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.
Area of Science:
- Neurogenetics
- Molecular Biology
- Ataxiology
Background:
- Spinocerebellar ataxia type 3 (SCA3) is a neurodegenerative disorder influenced by genetic factors.
- The ATXN2 gene, particularly its CAG repeat length and other variants like duplications, is implicated in SCA3 pathogenesis.
- Previous research has proposed ATXN2 variants as potential modifiers of SCA3 onset and progression.
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