DFNB16 is a frequent cause of congenital hearing impairment: implementation of STRC mutation analysis in routine diagnostics

por Vona, B, Hofrichter, MAH, Neuner, C, Schröder, J, Gehrig, A, Hennermann, JB, Kraus, F, Shehata-Dieler, W, Klopocki, E, Nanda, I, Haaf, T
Publicado 2015