A screening analysis of the GJB2 c.176 del 16 mutation responsible for hereditary deafness in a Chinese family

OBJECTIVE: To determine whether a new-born child from a family carrying a deafness gene needs cochlear implantation to avoid dysphonia by screening and sequencing a deafness-related gene. RESULTS: Both screening and sequencing results confirmed that the new born child had a normal GJB2 gene despite...

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Detalles Bibliográficos
Autores principales: Jiang, Hao, Shi, Xi, Qiu, Shiwei, Dong, Yanfen, Qiao, Yuehua, Wei, Dongzhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chinese PLA General Hospital 2016
Materias:
Research article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6002618/
https://www.ncbi.nlm.nih.gov/pubmed/29937822
http://dx.doi.org/10.1016/j.joto.2016.09.002

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6002618/
https://www.ncbi.nlm.nih.gov/pubmed/29937822
http://dx.doi.org/10.1016/j.joto.2016.09.002

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