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Detection of the GJB2 Mutation in Iranian Children with Hearing Loss Treated with Cochlear Implantation
The 35delG mutation in the gap junction protein, β2, 26kDa (GJB2) gene is the most common mutation that has been found in children with non syndromic hearing loss. Testing for the GJB2 gene mutation is simple and can directly answer the concerns of the parents about cause of the disorder and prognos...
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| Hoofdauteurs: | , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Macedonian Science of Sciences and Arts
2011
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3776689/ https://ncbi.nlm.nih.gov/pubmed/24052698 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2478/v10034-011-0013-4 |
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