Entrez 284403 | Ensembl ENSG00000075702 | |
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Aliases WDR62, C19orf14, MCPH2, WD repeat domain 62 External IDs MGI: 1923696 HomoloGene: 15927 GeneCards: WDR62 | ||
Clinical relevance
Mutations in the WDR62 gene cause of a wide spectrum of severe cerebral cortical malformations including microcephaly, pachygyria with cortical thickening, hypoplasia of the corpus callosum as well as polymicrogyria.
References
WDR62 Wikipedia(Text) CC BY-SA