TY  - GEN
AU  - Сhurbanov,Alexander Y
AU  - Karafet,Tatiana M
AU  - Morozov,Igor V
AU  - Mikhalskaia,Valeriia Yu
AU  - Zytsar,Marina V
AU  - Bondar,Alexander A
AU  - Posukh,Olga L
TI  - Whole Exome Sequencing Reveals Homozygous Mutations in RAI1, OTOF, and SLC26A4 Genes Associated with Nonsyndromic Hearing Loss in Altaian Families (South Siberia)
SN  - 1932-6203
PY  - 2016///0906
KW  - Cohort Studies
KW  - DNA Mutational Analysis
KW  - Deafness
KW  - genetics
KW  - Exome
KW  - Exons
KW  - Family Health
KW  - Female
KW  - Genetic Variation
KW  - Genome, Human
KW  - Geography
KW  - Homozygote
KW  - Humans
KW  - Male
KW  - Membrane Proteins
KW  - Membrane Transport Proteins
KW  - Mutation
KW  - Mutation, Missense
KW  - Pedigree
KW  - Siberia
KW  - Sulfate Transporters
KW  - Trans-Activators
KW  - Transcription Factors
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1371/journal.pone.0153841
ER  -