Functional assessment of allelic variants in the SLC26A4 gene involved in Pendred syndrome and nonsyndromic EVA. [electronic resource]
Producer: 20090107Description: 18608-13 p. digitalISSN:- 1091-6490
- Alleles
- Amino Acid Sequence
- Animals
- Cell Line
- Cohort Studies
- Genes, Recessive
- Genotype
- Hearing Loss, Sensorineural -- genetics
- Humans
- Membrane Transport Proteins -- genetics
- Molecular Sequence Data
- Mutation
- Open Reading Frames
- Phenotype
- Polymorphism, Genetic
- Sequence Homology, Amino Acid
- Sulfate Transporters
- Syndrome
- Vestibular Aqueduct -- abnormalities
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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