Ontology highlight
ABSTRACT:
SUBMITTER: Xu T
PROVIDER: S-EPMC6691240 | biostudies-literature | 2019 Sep
REPOSITORIES: biostudies-literature
Molecular medicine reports 20190715 3
The aim of the present study was to elucidate the role of the non‑syndromic autosomal recessive deafness 12 allelic variant of cadherin 23 (CDH23) in Chinese patients with non‑syndromic hearing loss. The present study focused on a Chinese family with hearing loss in which there were two siblings with autosomal, recessive deafness, ranging from severe to profound hearing loss over all frequencies. DNA sequencing was used to assess the genetic factors in the disease etiology. The data revealed a c ...[more]