Mutations in PTPRQ are a cause of autosomal-recessive nonsyndromic hearing impairment DFNB84 and associated with vestibular dysfunction. [electronic resource]
Producer: 20100422Description: 604-10 p. digitalISSN:- 1537-6605
- 5' Untranslated Regions -- genetics
- Amino Acid Sequence
- Case-Control Studies
- Codon, Nonsense -- genetics
- Cohort Studies
- Female
- Genes, Recessive
- Hearing Loss -- genetics
- Homozygote
- Humans
- Male
- Middle Aged
- Molecular Sequence Data
- Pedigree
- Polymorphism, Single Nucleotide -- genetics
- Receptor-Like Protein Tyrosine Phosphatases, Class 3 -- genetics
- Sequence Homology, Amino Acid
- Vestibular Diseases -- genetics
- Vestibular Function Tests
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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