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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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| Publicado no: | J Otol |
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| Principais autores: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Chinese PLA General Hospital
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6002618/ https://ncbi.nlm.nih.gov/pubmed/29937822 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.joto.2016.09.002 |
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