Functional null mutations of MSRB3 encoding methionine sulfoxide reductase are associated with human deafness DFNB74. [electronic resource]
Producer: 20110203Description: 19-29 p. digitalISSN:- 1537-6605
- Aged
- Animals
- Base Sequence
- Binding Sites -- genetics
- Carrier Proteins -- genetics
- Cohort Studies
- Deafness -- enzymology
- Ear, Inner -- enzymology
- Exons -- genetics
- Female
- Genes, Recessive
- Genetic Linkage
- Genetic Loci
- Hearing Loss -- genetics
- Homozygote
- Humans
- Male
- Methionine Sulfoxide Reductases
- Mice
- Middle Aged
- Mitochondrial Diseases -- enzymology
- Molecular Sequence Data
- Mutation
- Oxidoreductases Acting on Sulfur Group Donors -- genetics
- Polymorphism, Single Nucleotide
- White People -- genetics
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Publication Type: Journal Article
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