| Mutation spectrum of autosomal recessive non-syndromic hearing loss in central Iran Sep 3rd 2015, 01:32, by Asieh Haghighat-Nia, Azadeh Keivani, ZakiyeNadeali, Esmat Fazel-Najafabadi, Majid Hosseinzadeh, Mansoor Salehi To identify the spectrum of mutations in connexin 26 gene and frequency of two deletions in connexin 30 gene in central Iran. |
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