Homozygous and compound-heterozygous mutations in TGDS cause Catel-Manzke syndrome
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author: Gabriele Gillessen-Kaesbach, Almuth Caliebe, Valérie Cormier-Daire, Stefan Mundlos, Björn Fischer-Zirnsak, Celine Huber, Malte Spielmann, Peter Krawitz, Peter Nürnberg, Reiner Siebert, Janine Altmüller, Holger Thiele, Sarina G. Kant, Denise Horn, Zornitza Stark
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