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). - Teryutin, Fedor M.; Pshennikova, Vera G.; Solovyev, Aisen V.; Romanov, Georgii P.; Fedorova, Sardana A.; Barashkov, Nikolay A. (PLoS ONE, 2024)