The SLC26A4 c.706C>G (p.Leu236Val) variant is a frequent cause of hearing impairment in Filipino cochlear implantees

HYPOTHESIS: Variants in SLC26A4 are an important cause of congenital hearing impairment in the Philippines. BACKGROUND: Cochlear implantation is a standard rehabilitation option for congenital hearing impairment worldwide, but places a huge cost burden in lower-income countries. The study of risk fa...

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Publicat a:Otol Neurotol
Autors principals: Chiong, Charlotte M., Reyes-Quintos, Ma. Rina T., Yarza, Talitha Karisse L., Tobias-Grasso, Celina Ann M., Acharya, Anushree, Leal, Suzanne M., Mohlke, Karen L., Mayol, Nanette L., Cutiongco-de la Paz, Eva Maria, Santos-Cortez, Regie Lyn P.
Format: Artigo
Idioma:Inglês
Publicat: 2018
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6097524/
https://ncbi.nlm.nih.gov/pubmed/30113565
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MAO.0000000000001893
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