Targeted Mutation Analysis of the SLC26A4, MYO6, PJVK and CDH23 Genes in Iranian Patients with AR Nonsyndromic Hearing Loss. [electronic resource]
Producer: 20191212Description: 93-102 p. digitalISSN:- 1551-3823
- Adolescent
- Adult
- Cadherin Related Proteins
- Cadherins -- genetics
- Child
- Child, Preschool
- DNA Mutational Analysis -- methods
- Deafness -- diagnosis
- Female
- Gene Frequency -- genetics
- Hearing Loss -- genetics
- Humans
- Infant
- Iran
- Male
- Mutation -- genetics
- Myosin Heavy Chains -- genetics
- Nerve Tissue Proteins -- genetics
- Sulfate Transporters -- genetics
- Young Adult
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Publication Type: Journal Article
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