SCHRADERS, M. Et Al. 2012. Mutations of the Gene Encoding Otogelin Are a Cause of Autosomal-Recessive Nonsyndromic Moderate Hearing Impairment. AMERICAN JOURNAL OF HUMAN GENETICS , vol.91, no.5 , 883-889.

SCHRADERS, M., RUIZ-PALMERO, L., KALAY, E., OOSTRIK, J., DEL CASTILLO, F. J., SEZGIN, O., ... BEYNON, A. J.(2012). Mutations of the Gene Encoding Otogelin Are a Cause of Autosomal-Recessive Nonsyndromic Moderate Hearing Impairment. AMERICAN JOURNAL OF HUMAN GENETICS , vol.91, no.5, 883-889.

SCHRADERS, Margit Et Al. "Mutations of the Gene Encoding Otogelin Are a Cause of Autosomal-Recessive Nonsyndromic Moderate Hearing Impairment," AMERICAN JOURNAL OF HUMAN GENETICS , vol.91, no.5, 883-889, 2012

SCHRADERS, Margit Et Al. "Mutations of the Gene Encoding Otogelin Are a Cause of Autosomal-Recessive Nonsyndromic Moderate Hearing Impairment." AMERICAN JOURNAL OF HUMAN GENETICS , vol.91, no.5, pp.883-889, 2012

SCHRADERS, M. Et Al. (2012) . "Mutations of the Gene Encoding Otogelin Are a Cause of Autosomal-Recessive Nonsyndromic Moderate Hearing Impairment." AMERICAN JOURNAL OF HUMAN GENETICS , vol.91, no.5, pp.883-889.

@article{article, author={Margit SCHRADERS Et Al. }, title={Mutations of the Gene Encoding Otogelin Are a Cause of Autosomal-Recessive Nonsyndromic Moderate Hearing Impairment}, journal={AMERICAN JOURNAL OF HUMAN GENETICS}, year=2012, pages={883-889} }