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Scott, D.A., Kraft, M.L., Carmi, R., Ramesh, A., Elbedour, K., Yairi, Y., Srikumari Srisailapathy, C.R., Rosengren, S.S., Markham, A.F., Mueller, R.F., Lench, N.J., Van Camp, G., Smith, R.J.H. and Sheffield, V.C. (1998) Identification of mutation in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss. Human Mutation, 11, 387-394.
http://dx.doi.org/10.1002/(SICI)1098-1004(1998)11:5<387::AID-HUMU6>3.0.CO;2-8
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