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Estivill, X., Fortina, P., Surrey, S., Rabionet, R., Melchionda, S., D’Agruma, L., Mansfield, E., Rappaport, E., Govea, N., Mila, M., Zelante, L. and Gasparini, P. (1998) Connexin-26 mutations in sporadic and inherited sensorineural deafness. Lancet, 351, 394-398.
http://dx.doi.org/10.1016/S0140-6736(97)11124-2
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