<scp>DFNB16</scp> is a frequent cause of congenital hearing impairment: implementation of <i><scp>STRC</scp></i> mutation analysis in routine diagnostics
Barbara Vona(Brigham and Women's Hospital), Thomas Haaf(University of Würzburg), Cordula Neuner, Julia B. Hennermann(Charité - Universitätsmedizin Berlin), Eva Klopocki(University of Würzburg), Wafaa Shehata-Dieler, Fabian Kraus(LMU Klinikum), Jörg Schröder, I. Nanda, Andrea Gehrig(University of Würzburg), Michaela A. H. Hofrichter(University of Würzburg)
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