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)

• Fedor M. Teryutin,

  Roles Conceptualization, Writing – original draft

  Affiliation Laboratory of Molecular Genetics, Yakut Scientific Centre of Complex Medical Problems, Yakutsk, Russia

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• Vera G. Pshennikova,

  Roles Data curation, Investigation, Resources

  Affiliation Laboratory of Molecular Genetics, Yakut Scientific Centre of Complex Medical Problems, Yakutsk, Russia

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• Aisen V. Solovyev,

  Roles Formal analysis, Validation

  Affiliation Laboratory of Molecular Biology, Institute of Natural Sciences, M.K. Ammosov North-Eastern Federal University, Yakutsk, Russia

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• Georgii P. Romanov,

  Roles Formal analysis, Validation

  Affiliation Laboratory of Molecular Biology, Institute of Natural Sciences, M.K. Ammosov North-Eastern Federal University, Yakutsk, Russia

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• Sardana A. Fedorova,

  Roles Funding acquisition, Project administration, Writing – review & editing

  Affiliations Laboratory of Molecular Genetics, Yakut Scientific Centre of Complex Medical Problems, Yakutsk, Russia, Laboratory of Molecular Biology, Institute of Natural Sciences, M.K. Ammosov North-Eastern Federal University, Yakutsk, Russia

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• Nikolay A. Barashkov

  Roles Conceptualization, Funding acquisition, Supervision, Writing – original draft

  * E-mail: barashkov2004@mail.ru

  Affiliation Laboratory of Molecular Genetics, Yakut Scientific Centre of Complex Medical Problems, Yakutsk, Russia

  https://orcid.org/0000-0002-6984-7934

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