Common mutation analysis of GJB2 and GJB6 genes in affected families with autosomal recessive non-syndromic hearing loss from Iran: simultaneous detection of two common mutations (35delG/del(GJB6-D13S1830)) in the DFNB1-related deafness.
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| Description | scientific article published on 21 March 2007 |
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author: Mortaza Bonyadi |
| Publication date | March 21, 2007 |
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