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"Frequency of A Very Rare 35delG Mutation in Two Ethnic Groups of Iranian Populations "

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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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Main Authors:	R Sasanfar (Author), A Tolouei (Author), A Hoseinipour (Author), DD Farhud (Author), M Dolati (Author), L Hoghooghi Rad (Author), M Montazer Zohour (Author), M Ghadami (Author), H Pour-Jafari (Author), M Hashemzadeh Chaleshtori (Author)
Format:	Book
Published:	Tehran University of Medical Sciences, 2004-12-01T00:00:00Z.
Subjects:	article
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