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Whole Exome Sequencing Reveals Homozygous Mutations in RAI1, OTOF, and SLC26A4 Genes Associated with Nonsyndromic Hearing Loss in Altaian Families (South Siberia)
- Alexander Y. Сhurbanov,
- Tatiana M. Karafet,
- Igor V. Morozov,
- Valeriia Yu. Mikhalskaia,
- Marina V. Zytsar,
- Alexander A. Bondar,
- Olga L. Posukh
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- Published: April 15, 2016
- https://doi.org/10.1371/journal.pone.0153841