Mutations in WNT1 Cause Different Forms of Bone Fragility

Katharina Keupp(University of Cologne), Filippo Beleggia(University of Cologne), Hülya Kayserili(Istanbul University), Aileen M. Barnes(National Institutes of Health), Magdalena Steiner(Charité - Universitätsmedizin Berlin), Oliver Semler(University of Cologne), Björn Fischer‐Zirnsak(Charité - Universitätsmedizin Berlin), Gökhan Yigit(University of Cologne), Claudia Y. Janda(Howard Hughes Medical Institute), Jutta Becker(University of Cologne), Stefan Breer(Universität Hamburg), Umut Altunoğlu(Istanbul University), Johannes Grünhagen(Charité - Universitätsmedizin Berlin), Peter Krawitz(Charité - Universitätsmedizin Berlin), Jochen Hecht(Berlin-Brandenburger Centrum für Regenerative Therapien), Thorsten Schinke(Universität Hamburg), Elena Makareeva(National Institutes of Health), Ekkehart Lausch(University of Freiburg), Tufan Çankaya(Dokuz Eylül University), José A. Caparrós‐Martín(Consejo Superior de Investigaciones Científicas), Pablo Lapunzina(Hospital Universitario La Paz), Samia A. Temtamy(National Research Centre), Mona Aglan(National Research Centre), Bernhard Zabel(University of Freiburg), Peer Eysel(University of Cologne), Friederike Koerber(University of Cologne), Sergey Leikin(National Institutes of Health), K. Christopher García(Howard Hughes Medical Institute), Christian Netzer(University of Cologne), Eckhard Schönaü(University of Cologne), Víctor L. Ruiz‐Pérez(Consejo Superior de Investigaciones Científicas), Stefan Mundlos(Max Planck Institute for Molecular Genetics), Michael Amling(Universität Hamburg), Uwe Kornak(Max Planck Institute for Molecular Genetics), Joan C. Marini(National Institutes of Health), Bernd Wollnik(University of Cologne)
The American Journal of Human Genetics
March 14, 2013
Cited by 283Open Access
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