TY  - GEN
AU  - Anwar,Saima
AU  - Riazuddin,Saima
AU  - Ahmed,Zubair M
AU  - Tasneem,Saba
AU  - Khan,Shahid Y
AU  - Griffith,Andrew J
AU  - Friedman,Thomas B
AU  - Riazuddin,Sheikh
TI  - SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis
SN  - 1435-232X
PY  - 2010///0203
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Amino Acid Sequence
KW  - Case-Control Studies
KW  - Chromosomes, Human, Pair 7
KW  - Deafness
KW  - complications
KW  - Exons
KW  - Genetic Predisposition to Disease
KW  - Haplotypes
KW  - Homozygote
KW  - Humans
KW  - Membrane Transport Proteins
KW  - chemistry
KW  - Microsatellite Repeats
KW  - Molecular Sequence Data
KW  - Mutation
KW  - Pakistan
KW  - ethnology
KW  - Physical Chromosome Mapping
KW  - Polymorphism, Single Nucleotide
KW  - Sequence Alignment
KW  - Sulfate Transporters
KW  - Syndrome
N1  - Publication Type: Journal Article; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1038/jhg.2009.21
ER  -