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Detection of Connexion 26 GENE (GJB2) Mutations in Cases of Congenital Non Syndromic Deafness
Hearing loss is most common form of genetic hearing disorder. Non-syndromic sensory neural autosomal recessive deafness (NSRD) is the most common form of genetic hearing loss. Mutations in GJB2 gene, which encodes the connexin 26 protein, are major cause of NSRD. The aim of this study is directed to...
में बचाया:
| में प्रकाशित: | Indian J Otolaryngol Head Neck Surg |
|---|---|
| मुख्य लेखकों: | , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
Springer India
2015
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4899369/ https://ncbi.nlm.nih.gov/pubmed/27340645 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12070-015-0950-4 |
| टैग : |
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