ZSCAN10 deficiency causes a neurodevelopmental disorder with characteristic oto-facial malformations
Lucia Laugwitz(University Children's Hospital Tübingen), Tobias B. Haack(Technical University of Munich), Hamid Ghaedi(Shahid Beheshti University of Medical Sciences), Mina Zamani(Shahid Chamran University of Ahvaz), Binnaz Yalcin(Université de Bourgogne), Stéphanie Efthymiou(Istituto Giannina Gaslini), Samira Molaei Ramshe(Shahid Beheshti University of Medical Sciences), Sébastien Couette(Centre National de la Recherche Scientifique), Dirk Klee(Heinrich Heine University Düsseldorf), Marie Thirion(Inserm), Nuzhat Rana, Helen Cox(The Alfred Hospital), Saeid Sadeghian(Ahvaz Jundishapur University of Medical Sciences), Alireza Sedaghat(Ahvaz Jundishapur University of Medical Sciences), Mona Grimmel(University of Tübingen), David Murphy(National Hospital for Neurology and Neurosurgery), Aswinkumar Vijayananth(University of Bonn), A Ghamari Zare(Shahid Beheshti University of Medical Sciences), Fubo Cheng(Jilin University), Benjamin Bender(University of Tübingen), Alexander Hustinx(University of Bonn), Olaf Rieß(STZ eyetrial), Jawaher Zeighami, Rebecca Buchert(Institute of Human Genetics), Tzung‐Chien Hsieh(University of Bonn), Hamid Galehdari(Shahid Chamran University of Ahvaz), Dagmar Wieczorek(Essen University Hospital), Wenxu Zheng(University of Tübingen), Reza Azizi Malamiri(Ahvaz Jundishapur University of Medical Sciences), Ruth Falb(University of Tübingen), Henry Houlden(National Hospital for Neurology and Neurosurgery), Reza Maroofian(University of Exeter), Ute Grasshoff(University of Tübingen), Marc Sturm(University of Tübingen), Annette Seibt(Heinrich Heine University Düsseldorf), Nicolas Navarro(Centre National de la Recherche Scientifique), Stephan Ossowski(Max Planck Institute for Developmental Biology), Behnam Alipoor(Yasuj University of Medical Sciences), Ryan Gavin(Wessex Regional Genetics Laboratory), Simon Welsch(Heinrich Heine University Düsseldorf), Felix Dıstelmaıer(Heinrich Heine University Düsseldorf), Stephan C. Collins(Inserm), Faisal Zafar, Peter Krawitz(Institute of Human Genetics)
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