A KCNQ4 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 KCNQ4 gene is a common genetic factor of ADNSHL. Few studies have investigated the association between hearing impairment and the variant c.546C>G of KCNQ4. Here, we investigated the phen...

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Detalles Bibliográficos
Autores principales: Yen, Ting-Ting, Chen, I-Chieh, Hua, Men-Wei, Wei, Chia-Yi, Shih, Kai-Hsiang, Li, Jui-Lin, Lin, Ching-Heng, Hsiao, Tzu-Hung, Chen, Yi-Ming, Jiang, Rong-San
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8618107/
https://www.ncbi.nlm.nih.gov/pubmed/34828318
http://dx.doi.org/10.3390/genes12111711

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8618107/
https://www.ncbi.nlm.nih.gov/pubmed/34828318
http://dx.doi.org/10.3390/genes12111711

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