A novel KCNQ4 gene variant (c.857A>G; p.Tyr286Cys) in an extended family with non-syndromic deafness 2A

Deafness is one of the most common sensory disorders found in humans; notably, >60% of all cases of deafness have been attributed to genetic factors. Variants in potassium voltage-gated channel subfamily Q member 4 (KCNQ4) are etiologically linked to a type of progressive hearing loss, deafness n...

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Detalles Bibliográficos
Autores principales: Li, Qiong, Liang, Pengfei, Wang, Shujuan, Li, Wei, Wang, Jian, Yang, Yang, An, Xiaogang, Chen, Jun, Zha, Dingjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2021
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8025472/
https://www.ncbi.nlm.nih.gov/pubmed/33846771
http://dx.doi.org/10.3892/mmr.2021.12059

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8025472/
https://www.ncbi.nlm.nih.gov/pubmed/33846771
http://dx.doi.org/10.3892/mmr.2021.12059

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