Whole exome sequencing reveals homozygous mutations in RAI1, OTOF, and SLC26A4 genes associated with nonsyndromic hearing loss in Altaian families (South Siberia)

Alexander Y. Churbanov, Tatiana M. Karafet, Igor V. Morozov, Valeriia Yu Mikhalskaia, Marina V. Zytsar, Alexander A. Bondar, Olga L. Posukh

Research output: Contribution to journal › Article › peer-review

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Medicine & Life Sciences