Confirmation of diagnosis in Romanian children with DFNB1 related hearing loss

来源 :美国分子生物学期刊(英文) | 被引量 : 0次 | 上传用户:jiaolang
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DFNB1 locus has been linked to a nonsyndromic “invisible disability” called congenital sensorineural hearing loss and deafness. Mutations of GJB2 and GJB6 genes are associated with deafness at the DFNB1 locus. The diagnosis of DFNB1 is made with molecular
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