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Teryutin FM, Pshennikova VG, Solovyev AV, Romanov GP, et al. 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). PLoS One 2024;19:e0309439.
PMID: 39436953


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