Temtamy Preaxial Brachydactyly Syndrome Is Caused by Loss-of-Function Mutations in Chondroitin Synthase 1, a Potential Target of BMP Signaling

Yun Li(University of Cologne), Kathrin Laue(University of Cologne), Samia A. Temtamy(National Research Centre), Mona Aglan(National Research Centre), Leman Damla Kotan(Cukurova University), Gökhan Yigit(University of Cologne), Husniye Canan(Cukurova University), Barbara Pawlik(University of Cologne), Gudrun Nürnberg(University of Cologne), Emma Wakeling(Wessex Regional Genetics Laboratory), Oliver Quarrell(Sheffield Children's Hospital), Ingelore Baessmann(University of Cologne), Matthew B. Lanktree(Western University), M. Yılmaz(Cukurova University), Robert A. Hegele(Western University), Khalda Amr(National Research Centre), Klaus W. May(Software (Germany)), Peter Nürnberg(University of Cologne), A. Kemal Topaloğlu(Cukurova University), Matthias Hammerschmidt(University of Cologne), Bernd Wollnik(University of Cologne)
The American Journal of Human Genetics
December 1, 2010
Cited by 96Open Access
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