ArticleOncotarget2016

Novel mutations c.28G>T (p.Ala10Ser) and c.189G>T (p.Glu63Asp) in WDR62 associated with early onset acanthosis and hyperkeratosis in a patient with autosomal recessive microcephaly type 2.

Santasree Banerjee et al.PubMed ↗Full text ↗Publisher ↗

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