SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis. [electronic resource]
Producer: 20100203Description: 266-70 p. digitalISSN:- 1435-232X
- Abnormalities, Multiple -- genetics
- Amino Acid Sequence
- Case-Control Studies
- Chromosomes, Human, Pair 7 -- genetics
- Deafness -- complications
- Exons -- genetics
- Genetic Predisposition to Disease
- Haplotypes -- genetics
- Homozygote
- Humans
- Membrane Transport Proteins -- chemistry
- Microsatellite Repeats -- genetics
- Molecular Sequence Data
- Mutation -- genetics
- Pakistan -- ethnology
- Physical Chromosome Mapping
- Polymorphism, Single Nucleotide -- genetics
- Sequence Alignment
- Sulfate Transporters
- Syndrome
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Publication Type: Journal Article; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't
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