Sineni, C. J. Et Al. 2019. A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss. Human Genetics , vol.138, no.10 , 1071-1075.

Sineni, C. J., Yildirim-Baylan, M., Guo, S., Camarena, V., Wang, G., TOKGÖZ YILMAZ, S., ... DUMAN, D.(2019). A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss. Human Genetics , vol.138, no.10, 1071-1075.

Sineni, Claire Et Al. "A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss," Human Genetics , vol.138, no.10, 1071-1075, 2019

Sineni, Claire J. Et Al. "A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss." Human Genetics , vol.138, no.10, pp.1071-1075, 2019

Sineni, C. J. Et Al. (2019) . "A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss." Human Genetics , vol.138, no.10, pp.1071-1075.

@article{article, author={Claire J. Sineni Et Al. }, title={A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss}, journal={Human Genetics}, year=2019, pages={1071-1075} }