Copy-number variation of the neuronal glucose transporter gene SLC2A3 and age of onset in Huntington's disease.

Hum Mol Genet · 2014 · PMC4030768 · PMID 24452335

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modest significanceno p-value reported

The modest significance value reflects the small overall effect on AO in the HD population, and this is due to the low frequency of the deletion (0.25%) and duplication alleles (1.9%).

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