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Zelante, L., Gasparini, P., Estivill, X., Melchionda, S., D’Agruma, L., Govea, N., Mila, M., Monica, M.D., Lutfi, J., Shohat, M., Manfield, E., Delgroso, K., Rappaport, E., Surrey, S. and Fortina, P. (1997) Connexin 26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans. Human Molecular Genetics, 6, 1605-1609.
http://dx.doi.org/10.1111/j.1749-6632.1991.tb19572.x
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