ZC4H2 Mutations Are Associated with Arthrogryposis Multiplex Congenita and Intellectual Disability through Impairment of Central and Peripheral Synaptic Plasticity

Hiromi Hirata; Indrajit Nanda; Anne van Riesen; G. McMichael; Hao Hu; M Hambrock; Marie-Amélie Papon; Ute Fischer; Sylviane Marouillat; Can Ding; Servane Alirol; Melanie Bienek; Sabine Preisler-Adams; Astrid Grimme; Dominik Seelow; Richard Webster; Eric Haan; Alastair H. MacLennan; Werner Stenzel; Tzu Ying Yap; Alison Gardner; Lam Son Nguyen; Marie Shaw; Nicolas Lebrun; Stefan A. Haas; Wolfram Kreß; Thomas Haaf; Elke Schellenberger; Jamel Chelly; Géraldine Viot; Lisa G. Shaffer; Jill A. Rosenfeld; Nancy Kramer; Rena E. Falk; Dima El‐Khechen; Luis Escobar; Raoul C. M. Hennekam; Peter Wieacker; Christoph Hübner; Hans‐Hilger Ropers; Jozef Gécz; Markus Schuelke; Frédéric Laumonnier; Vera M. Kalscheuer

doi:10.1016/j.ajhg.2013.03.021

ZC4H2 Mutations Are Associated with Arthrogryposis Multiplex Congenita and Intellectual Disability through Impairment of Central and Peripheral Synaptic Plasticity

Hiromi Hirata(National Institute of Genetics), Indrajit Nanda(University of Würzburg), Anne van Riesen(Charité - Universitätsmedizin Berlin), G. McMichael(The University of Adelaide), Hao Hu(Max Planck Institute for Molecular Genetics), M Hambrock(Max Planck Institute for Molecular Genetics), Marie-Amélie Papon(Université de Tours), Ute Fischer(Max Planck Institute for Molecular Genetics), Sylviane Marouillat(Université de Tours), Can Ding(Charité - Universitätsmedizin Berlin), Servane Alirol(Université de Tours), Melanie Bienek(Max Planck Institute for Molecular Genetics), Sabine Preisler-Adams(University of Münster), Astrid Grimme(Max Planck Institute for Molecular Genetics), Dominik Seelow(Charité - Universitätsmedizin Berlin), Richard Webster(Children's Hospital at Westmead), Eric Haan(South Australia Pathology), Alastair H. MacLennan(The University of Adelaide), Werner Stenzel(Charité - Universitätsmedizin Berlin), Tzu Ying Yap(The University of Adelaide), Alison Gardner(South Australia Pathology), Lam Son Nguyen(The University of Adelaide), Marie Shaw(The University of Adelaide), Nicolas Lebrun(Délégation Paris 5), Stefan A. Haas(Max Planck Institute for Molecular Genetics), Wolfram Kreß(University of Würzburg), Thomas Haaf(University of Würzburg), Elke Schellenberger(Universitäts-Kinderklinik Würzburg), Jamel Chelly(Délégation Paris 5), Géraldine Viot(Hôpital Cochin), Lisa G. Shaffer(PerkinElmer (United States)), Jill A. Rosenfeld(PerkinElmer (United States)), Nancy Kramer(Cedars-Sinai Medical Center), Rena E. Falk(Cedars-Sinai Medical Center), Dima El‐Khechen(Peyton Manning Children’s Hospital at St.Vincent), Luis Escobar(Peyton Manning Children’s Hospital at St.Vincent), Raoul C. M. Hennekam(Amsterdam UMC Location University of Amsterdam), Peter Wieacker(University of Münster), Christoph Hübner(Charité - Universitätsmedizin Berlin), Hans‐Hilger Ropers(Max Planck Institute for Molecular Genetics), Jozef Gécz(South Australia Pathology), Markus Schuelke(Charité - Universitätsmedizin Berlin), Frédéric Laumonnier(Université de Tours), Vera M. Kalscheuer(Max Planck Institute for Molecular Genetics)

The American Journal of Human Genetics

April 25, 2013

10.1016/j.ajhg.2013.03.021

Cited by 90Open Access

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