Whole Exome Sequencing Reveals Homozygous Mutations in RAI1, OTOF, and SLC26A4 Genes Associated with Nonsyndromic Hearing Loss in Altaian Families (South Siberia)-Reference-Cited by-同舟云学术

Whole Exome Sequencing Reveals Homozygous Mutations in RAI1, OTOF, and SLC26A4 Genes Associated with Nonsyndromic Hearing Loss in Altaian Families (South Siberia)

Published:2016-04-15 Issue:4 Volume:11 Page:e0153841
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

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

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference65 articles.

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