机译:A common founder effect of the splice site variant c.-23?+?1G??A in GJB2 gene causing autosomal recessive deafness 1A (DFNB1A) in Eurasia
Laboratory of Molecular Biology, Institute of Natural Sciences,M.K. Ammosov North-Eastern Federal;
Research Centre for Medical Genetics;
Estonian Biocentre, Institute of Genomics,University of TartuFederal Research Center Institute of Cytology and Genetics,Siberian Branch of the Russian AcademyLaboratory of Molecular Genetics,Yakut Science Centre of Complex Medical ProblemsNational Research Centre for Audiology and Hearing RehabilitationInstitute of Molecular Biomedicine,Comenius University Faculty of MedicineInstitute of Molecular Physiology and Genetics,Slovak Academy of Sciences;