TY  - GEN
AU  - Ahmed,Zubair M
AU  - Yousaf,Rizwan
AU  - Lee,Byung Cheon
AU  - Khan,Shaheen N
AU  - Lee,Sue
AU  - Lee,Kwanghyuk
AU  - Husnain,Tayyab
AU  - Rehman,Atteeq Ur
AU  - Bonneux,Sarah
AU  - Ansar,Muhammad
AU  - Ahmad,Wasim
AU  - Leal,Suzanne M
AU  - Gladyshev,Vadim N
AU  - Belyantseva,Inna A
AU  - Van Camp,Guy
AU  - Riazuddin,Sheikh
AU  - Friedman,Thomas B
AU  - Riazuddin,Saima
TI  - Functional null mutations of MSRB3 encoding methionine sulfoxide reductase are associated with human deafness DFNB74
SN  - 1537-6605
PY  - 2011///0203
KW  - Aged
KW  - Animals
KW  - Base Sequence
KW  - Binding Sites
KW  - genetics
KW  - Carrier Proteins
KW  - Cohort Studies
KW  - Deafness
KW  - enzymology
KW  - Ear, Inner
KW  - Exons
KW  - Female
KW  - Genes, Recessive
KW  - Genetic Linkage
KW  - Genetic Loci
KW  - Hearing Loss
KW  - Homozygote
KW  - Humans
KW  - Male
KW  - Methionine Sulfoxide Reductases
KW  - Mice
KW  - Middle Aged
KW  - Mitochondrial Diseases
KW  - Molecular Sequence Data
KW  - Mutation
KW  - Oxidoreductases Acting on Sulfur Group Donors
KW  - Polymorphism, Single Nucleotide
KW  - White People
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1016/j.ajhg.2010.11.010
ER  -