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特許 係属中 WD repeat-containing protein 62 is a protein that in humans is encoded by the WDR62 gene. Mutations in the WDR62 gene cause of a wide spectrum of severe cerebral cortical malformations including microcephaly,[3] pachygyria with cortical thickening, hypoplasia of the corpus callosum[1] as well as polymicrogyria.
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