La mutation 35delG du gène de la connexine 26, une cause...

La mutation 35delG du gène de la connexine 26, une cause fréquente des surdités non syndromiques autosomiques récessives au Maroc

I. Ratbi, S. Hajji, K. Ouldim, N. Aboussair, D. Feldmann, A. Sefiani
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Volume:
14
Year:
2007
Language:
french
Pages:
454
DOI:
10.1016/j.arcped.2006.12.004
File:
PDF, 241 KB
french, 2007
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