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Article

Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation in WNT10A

25 Mar 2010

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 20418069
DOI: 10.1016/j.jdermsci.2010.03.012

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Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation in WNT10APMID 20418069Read ↗

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Clinical features and WNT10A mutations in seven unrelated cases of Schöpf-Schulz-Passarge syndrome.Semantic proximity Read ↗

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