A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans
Barbara Vona(Broad Institute), Hamid Galehdari(Shahid Chamran University of Ahvaz), Shruthi VijayKumar(Oklahoma Medical Research Foundation), Franz Rüschendorf(Max Delbrück Center), Richard J. Smith(University of Iowa), Thomas Haaf(Unknown), Sheng‐Jia Lin(Oklahoma Medical Research Foundation), A. Amraoui(Centre National de la Recherche Scientifique), Alireza Sedaghat(Ahvaz Jundishapur University of Medical Sciences), David Murphy(National Hospital for Neurology and Neurosurgery), Sandrine Vitry(Inserm), Kevin T. Booth(Indiana University School of Medicine), Héla Azaiez(University of Iowa), Neda Mazaheri(Shahid Chamran University of Ahvaz), Lucy A Dunbar(Mary Lyon Centre at MRC Harwell), Abolfazl Rad(Sabzevar University of Medical Sciences), Pratishtha Varshney(Oklahoma Medical Research Foundation), Henry Houlden(University College London), Reza Maroofian(National Hospital for Neurology and Neurosurgery), Cassidy Petree(Oklahoma Medical Research Foundation), Gholamreza Shariati(Ahvaz Jundishapur University of Medical Sciences), Christian Beetz(Jena University Hospital), Ben Fowler(Oklahoma Medical Research Foundation), Gaurav K. Varshney(Oklahoma Medical Research Foundation), Kumar N. Alagramam(University Hospitals of Cleveland), Michael R. Bowl(Mary Lyon Centre at MRC Harwell)
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