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    Genotype-phenotype analysis of hearing function in patients with DFNB1A caused by the c.-23+1G>A splice site variant of the GJB2 gene (Cx26).

    Genotype-phenotype analysis of hearing function in patients with DFNB1A caused by the c.-23+1G>A splice site variant of the GJB2 gene (Cx26). by Fedor M Teryutin, Vera G Pshennikova, Aisen V Solovyev, Georgii P Romanov, Sardana A Fedorova, Nikolay A Barashkov

    Published 2024-01-01
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