"Frequency of A Very Rare 35delG Mutation in Two Ethnic Groups of Iranian Populations "
The 35delG mutation in the Connexin 26 gene (Cx26), at the DNFB1 locus is the most common mutation in the patients with autosomal recessive non-syndromic hearing loss (ARNSHL). We have studied a total of 224 deaf cases from 189 families in two populations of Iran (Sistan va Bluchestan and Hormozgan...
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| Autors principals: | , , , , , , , , , |
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| Format: | Llibre |
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Tehran University of Medical Sciences,
2004-10-01T00:00:00Z.
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A1234.567 |
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