Genetics of Hearing Loss in North Iran Population: An Update of Spectrum and Frequency of GJB2 Mutations

Diagnosis of pre-lingual hearing loss (HL) is difficult owing to the high number of genes responsible. The most frequent cause of HL is DFNB1 due to mutations in the GJB2 gene. It represents up to 40% of HL cases in some populations. In Iran, it has previously been shown that DFNB1 accounts for 16-1...

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Detalles Bibliográficos
Autores principales: Koohiyan, Mahbobeh, Azadegan-Dehkordi, Fatemeh, Koohian, Farideh, Hashemzadeh-Chaleshtori, Morteza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Audiological Society and Korean Otological Society 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6773957/
https://www.ncbi.nlm.nih.gov/pubmed/31569309
http://dx.doi.org/10.7874/jao.2019.00059

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6773957/
https://www.ncbi.nlm.nih.gov/pubmed/31569309
http://dx.doi.org/10.7874/jao.2019.00059

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