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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.
Abstract
No abstract available in PubMed .
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