搜索结果: 1-1 共查到“基础医学 hearing”相关记录1条 . 查询时间(0.065 秒)
Autosomal Recessive and Sporadic Non Syndromic Hearing Loss and the Incidence of Cx26 Mutations in a Province of Iran
Connexin 26 GJB2 Deafness Autosomal recessive non syndromic hearing loss Iran
2010/2/4
Despite the enormous heterogeneity of genetic hearing loss, mutations in the GJB2 (connexin 26) gene located on “DFNB1” locus (13q12) account for up to 50% of cases of autosomal recessive non-syndromi...