Researchers find mutation responsible for deafness and hearing loss in Usher syndrome.

Researchers have pinpointed a new genetic mutation responsible for deafness and hearing loss in a condition called Usher syndrome type 1.

Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48 : Nature Genetics : Nature Publishing Group

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