Frequency of Connexin26 Gene Mutations in Autosomal Recessive Non-syndromic Deafness in Kermanshah(2002-4)
| Author | N Mahdieh | en |
| Author | C Nishimura | en |
| Author | K Ali-Madadi | en |
| Author | Y Yazdan | en |
| Author | S Kazemi | en |
| Author | Y Riazalhosseini | en |
| Author | S Arzhangi | en |
| Author | N Bazazadegan | en |
| Author | M Totonchi | en |
| Author | RJH Smith | en |
| Author | H Najmabadi | en |
| Issued Date | 2005-09-20 | en |
| Abstract | Introduction: Hearing loss is the most common sensory defect in humans, affecting approximately 1 in 1000 neonates in which genetic factors are involved in more than 50%. Connexin 26 or GJB2 gene mutations are responsible for half of autosomal recessive non-syndromic hearing losses. The purpose of this study was to determine the GJB2 mutations frequency in autosomal recessive non-syndromic deafness in Kermanshah. | en |
| DOI | https://doi.org/ | en |
| Keyword | 35delG | en |
| Keyword | GJB2 | en |
| Keyword | Autosomal Recessive Non-Syndromic Deafness | en |
| Keyword | Kermanshah | en |
| Publisher | Brieflands | en |
| Title | Frequency of Connexin26 Gene Mutations in Autosomal Recessive Non-syndromic Deafness in Kermanshah(2002-4) | en |
| Type | Research Article | en |
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