A <i>KCNQ4</i> c.546C>G Genetic Variant Associated with Late Onset Non-Syndromic Hearing Loss in a Taiwanese Population

A <i>KCNQ4</i> c.546C>G Genetic Variant Associated with Late Onset Non-Syndromic Hearing Loss in a Taiwanese Population

Clinical presentation is heterogeneous for autosomal dominant nonsyndromic hearing loss (ADNSHL). Variants of <i>KCNQ4</i> gene is a common genetic factor of ADNSHL. Few studies have investigated the association between hearing impairment and the variant c.546C>G of <i>KCNQ4<...

Full description

Saved in:
Bibliographic Details
Main Authors: Ting-Ting Yen, I-Chieh Chen, Men-Wei Hua, Chia-Yi Wei, Kai-Hsiang Shih, Jui-Lin Li, Ching-Heng Lin, Tzu-Hung Hsiao, Yi-Ming Chen, Rong-San Jiang
Format: article
Language:EN
Published: MDPI AG 2021
Subjects:
autosomal dominant nonsyndromic hearing loss
<i>KCNQ4</i> c.546C>G
audiograms
pure tone audiometry
Genetics
QH426-470
Online Access:https://doaj.org/article/28dc68c00be747efabc5e17a65a6a6e1
Tags: Add Tag
No Tags, Be the first to tag this record!

Internet

https://doaj.org/article/28dc68c00be747efabc5e17a65a6a6e1

Similar Items