Thirty-one different mutations were identified in GJB2 and GJB6 in 86 of the 252 (34%) patients. ![]() This article presents a mutation analysis of the GJB2, GJB6, OTOF and MTRNR1 genes in 252 patients with sensorineural non-syndromic hearing loss. Abstract Mutations in the GJB2 gene are responsible for more than half of all cases of recessive non-syndromic deafness.
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