Targeted sequencing of CDH23 and GJB2 genes in an Iranian pedigree with Usher syndrome and non-syndromic hearing loss.

Targeted sequencing of CDH23 and GJB2 genes in an Iranian pedigree with Usher syndrome and non-syndromic hearing loss.  Gene Reports (2021). Article Note: Otogenetics performed the Deafness gene test and identified the familial mutations for Usher syndrome and non-syndromic hearing loss.