Extension of the clinical and molecular phenotype of DIAPH1-associated autosomal dominant hearing loss ( DFNA1). - Neuhaus, C.; Lang‐Roth, R.; Zimmermann, U.; Heller, R.; Eisenberger, T.; Weikert, M.; Markus, S.; Knipper, M.; Bolz, H.J. (Clinical Genetics, 2017)