Phenotypic analyses and mutation screening of the SLC26A4 and FOXI1 genes in 101 Taiwanese families with bilateral nonsyndromic enlarged vestibular aqueduct (DFNB4) or Pendred syndrome. [electronic resource]
Producer: 20100219Description: 57-66 p. digitalISSN:- 1421-9700
- Alleles
- Audiometry
- Forkhead Transcription Factors -- genetics
- Genetic Testing
- Genotype
- Goiter -- genetics
- Hearing Loss -- genetics
- Humans
- Membrane Transport Proteins -- genetics
- Mutation
- Phenotype
- Polymorphism, Single Nucleotide -- genetics
- Promoter Regions, Genetic -- genetics
- Reverse Transcriptase Polymerase Chain Reaction
- Sulfate Transporters
- Syndrome
- Taiwan
- Vestibular Aqueduct -- pathology
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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