Barely Significant
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Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystonia.

Ann Neurol · 2013 · PMC3698699 · PMID 23424103

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highly significantno p-value reported
21 We report the identification of genetic linkage in this family to chromosome 19p13.12-13 with a highly significant LOD score of 6.33.

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