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, 2017-06, Vol.91 (6), p.892-901 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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