GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2-35delG mutation.
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| Description | scientific article |
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author: Redouane Boulouiz Abdelaziz Chafik Abdelaziz Tlili Abdelhamid Barakat Hassan Rouba Omar Abidi |
| Publication date | June 5, 2007 |
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