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Ein Fall von Schöpf-Schulz-Passarge-Syndrom verursacht durch eine c.1135C>T WNT10A Missense-Mutation

Clemens Painsi¹, Kristina Aubell², Peter Wolf³

¹Abteilung für Dermatologie und Venerologie, Klinikum Klagenfurt, Klagenfurt am Wörthersee, Österreich.

Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG

|April 6, 2017

Abstract

No abstract available in PubMed .

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