Functional null mutations of MSRB3 encoding methionine sulfoxide reductase are associated with human deafness DFNB74.

Ahmed, Zubair M

Functional null mutations of MSRB3 encoding methionine sulfoxide reductase are associated with human deafness DFNB74. [electronic resource] - American journal of human genetics Jan 2011 - 19-29 p. digital

Publication Type: Journal Article

1537-6605

10.1016/j.ajhg.2010.11.010 doi


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