Whole Exome Sequencing Reveals Homozygous Mutations in RAI1, OTOF, and SLC26A4 Genes Associated with Nonsyndromic Hearing Loss in Altaian Families (South Siberia). [electronic resource]
Producer: 20160906Description: e0153841 p. digitalISSN:- 1932-6203
- Cohort Studies
- DNA Mutational Analysis
- Deafness -- genetics
- Exome
- Exons
- Family Health
- Female
- Genetic Variation
- Genome, Human
- Geography
- Homozygote
- Humans
- Male
- Membrane Proteins -- genetics
- Membrane Transport Proteins -- genetics
- Mutation
- Mutation, Missense
- Pedigree
- Siberia
- Sulfate Transporters
- Trans-Activators
- Transcription Factors -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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