Ersan Kalay
Department of Human Genetics
Radboud University Nijmegen Medical Centre
P.O. Box 9101
6500 HB
Netherlands
Name/email consistency: high
- GJB2 mutations in Turkish patients with ARNSHL: prevalence and two novel mutations. Kalay, E., Caylan, R., Kremer, H., de Brouwer, A.P., Karaguzel, A. Hear. Res. (2005)
- Four novel TMC1 (DFNB7/DFNB11) mutations in Turkish patients with congenital autosomal recessive nonsyndromic hearing loss. Kalay, E., Karaguzel, A., Caylan, R., Heister, A., Cremers, F.P., Cremers, C.W., Brunner, H.G., de Brouwer, A.P., Kremer, H. Hum. Mutat. (2005)