The contribution of autosomaul recessive non-syndromic deafness to DFNB59 mutations (Pejvakin)
| Author | Marzieh Abolhasani | en |
| Author | Effat Farrokhi | en |
| Author | Mohsen Noorbakhsh | en |
| Author | Maryam Taherzadeh | en |
| Author | Fatemeh Azadegan | en |
| Author | Azam Asgari | en |
| Author | Morteza Hashmzadeh | en |
| Issued Date | 2010-10-31 | en |
| Abstract | Background : Hearing loss is a common disorder affecting millions of individuals worldwide with opproximately 1 in 1000 newborns. A novel gene, DFNB59 encods Pejvakin has been recently shown to cause neural deafness. The aim of this study was to determine the frequency of DFNB59 gene mutations in 93 deaf pupils in Sistan & Baluchestan province. | en |
| DOI | https://doi.org/ | en |
| Keyword | PCR-SSCP | en |
| Keyword | heteroduplex analysis | en |
| Keyword | pejvakin | en |
| Keyword | deafness | en |
| Publisher | Brieflands | en |
| Title | The contribution of autosomaul recessive non-syndromic deafness to DFNB59 mutations (Pejvakin) | en |
| Type | Research Article | en |
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