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American Journal of Human Genetics|May 11, 2010
A truncating mutation in SERPINB6 is associated with autosomal-recessive nonsyndromic sensorineural hearing lossAsli Sirmaci, Seyra Erbek, Justin Price, et al.
American Journal of Human Genetics|November 6, 2012
Mutations in OTOGL, encoding the inner ear protein otogelin-like, cause moderate sensorineural hearing lossKemal O Yariz, Duygu Duman, Celia Zazo Seco, et al.
Nature Genetics|October 2, 2012
Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48Saima Riazuddin, Inna A Belyantseva, Arnaud P J Giese, et al.
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