Barely Significant
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MSH3 is a genetic modifier of somatic repeat instability in X-linked dystonia parkinsonism.

Am J Hum Genet · 2026 · PMC12824618 · PMID 41443196

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nominally significantno p-value reported
Although there were some nominally significant associations, none of these genes showed significant associations after Bonferroni correction with contraction or AAO ( Tables S14 and S15 ).

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