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