DFNB16 is a frequent cause of congenital hearing impairment: implementation of STRC mutation analysis in routine diagnostics
Vona, B., Hofrichter, M.A.H., Neuner, C., Schröder, J., Gehrig, A., Hennermann, J.B., Kraus, F., Shehata-Dieler, W., Klopocki, E., Nanda, I., Haaf, T.
Published in Clinical genetics (01.01.2015)
Published in Clinical genetics (01.01.2015)
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