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    The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population

    Connexin 26 (GJB2) mutations lead to hearing loss in a significant proportion of all populations studied so far, despite the fact that at least 50 other genes are also associated with hearing loss. The entire co...

    T. Sobe, S. Vreugde, H. Shahin, M. Berlin, N. Davis, M. Kanaan, Y. Yaron… in Human Genetics (2000)