Genetics of hereditary hearing loss in east Iran population: A systematic review of GJB2 mutations

Mutations in the GJB2 gene are the most common cause of pre-lingual hearing loss (HL) worldwide. Previous studies have shown the frequency of GJB2 mutations to be 16% in Iran, but varies among different ethnic groups. Here, we have reviewed results from previous published mutation reports to provide...

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Vydáno v:Intractable Rare Dis Res
Hlavní autoři: Koohiyan, Mahbobeh, Azadegan-Dehkordi, Fatemeh, Koohian, Farideh, Abolhasani, Marziye, Hashemzadeh-Chaleshtori, Morteza
Médium: Artigo
Jazyk:Inglês
Vydáno: International Research and Cooperation Association for Bio & Socio-Sciences Advancement 2019
Témata:
Review
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6743427/
https://ncbi.nlm.nih.gov/pubmed/31523594
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5582/irdr.2019.01070
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