Mutations in CIB2 calcium and integrin-binding protein disrupt auditory hair cell calcium homeostasis in Usher syndrome type 1J and non-syndromic deafness DFNB48

Authors


e-mail: ajan@cmmt.ubc.ca

Abstract

Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and non-syndromic deafness DFNB48

Riazuddin et al. (2012)

Nature Genetics 44(11):1265–1271

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