Autosomal recessive non-syndromic hearing loss in the Lebanese population: prevalence of the 30delG mutation and report of two novel mutations in the connexin 26 (GJB2) gene. (Q43075593)
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scientific article published in October 2001
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Autosomal recessive non-syndromic hearing loss in the Lebanese population: prevalence of the 30delG mutation and report of two novel mutations in the connexin 26 (GJB2) gene. |
scientific article published in October 2001 |
Statements
Autosomal recessive non-syndromic hearing loss in the Lebanese population: prevalence of the 30delG mutation and report of two novel mutations in the connexin 26 (GJB2) gene (English)
M Mustapha
N Salem
E Chouery
M Ghassibeh
M Rai
J Loiselet
1 October 2001