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 High frequency of the p.R34X mutation in the TMC1 gene associated with nonsyndromic hearing loss is due to founder effects. Genet Test Mol Biomarkers. 2010 Jun;14(3):307-11
de Mariem ben said, Hmani-Aifa M., Amar I., Baig SM., Mustapha M., Delmaghani S., Tlili A., Ghorbel A., Ayadi H., Van Camp G., Smith RJ., Tekin M., Masmoudi S
2010 Résumé
Références
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