The prevalence and clinical characteristics of TECTA-associated autosomal dominant hearing loss.
TECTA is well known as the causative gene for autosomal dominant mid-frequency hearing loss observed in various populations. In this study, we performed next-generation sequencing analysis of a large Japanese hearing loss cohort from unrelated autosomal dominant hearing loss families, to estimate the prevalence and phenotype-genotype correlations in patients with TECTA mutations.
- Type: Case Set
- Archiver: Japanese Genotype-phenotype Archive (JGA)