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Mutations in GJB1, GJB2, GJB3 and GJB6 are involved in hearing impairment. GJB2, GJB3 and GJB6 are also mutated in patients with hyperproliferative skin disorders. The human GJB4 gene has been… Continue Reading
To the Editor: Late-onset deafness is likely to be the result of complex interactions between genetic susceptibility factors and the environment. Although enormous progress is being achieved in… Continue Reading