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Article

Schöpf-Schulz-Passarge syndrome associated with two new missense mutations in WNT10A.

Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG - 1 Jan 2018

Pauly Karolin Juliane, Balakirski Galina, Megahed Mosaad, Rübben Albert, Schmitt Laurenz

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Share to Anodontia
Share to Diagnosis, Differential
Share to Heterozygote
Share to Hypotrichosis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Keratoderma, Palmoplantar

Share to Mutation, Missense

Share to Phenotype

Share to Wnt Proteins

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Identifiers

PMID: 29314690
DOI: 10.1111/ddg.13391

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

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Schöpf-Schulz-Passarge syndrome associated with two new missense mutations in WNT10A.PMID 29314690Read ↗

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