A case report of non-syndromic sensorineural hearing loss with a compound heterozygous mutation (35delG/del120E) in the GJB2 gene
Hearing loss is one of the most common sensorineural disorders that occur in 1:1000. Mutation in the GJB2 (CX26) gene at the DFNB1 locus on chromosome 13q12 is the most important cause of congenital hearing loss. The aim of this study was to determine the hearing loss causative mutations in the GJB2...
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| Format: | Article |
| Language: | fas |
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Qazvin University of Medical Sciences & Health Services
2016-04-01
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| Series: | The Journal of Qazvin University of Medical Sciences |
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| Online Access: | http://journal.qums.ac.ir/browse.php?a_id=1959&slc_lang=fa&sid=1&ftxt=1 |