A. Alvarez, I. Del-castillo, M. Villamar, L. A. Aguirre, A. Gonzalez-neira et al., High prevalence of the W24X mutation in the gene encoding connexin-26 (GJB2) in Spanish Romani (gypsies) with autosomal recessive nonsyndromic hearing loss, Am. J. Med. Genet, vol.137, pp.255-258, 2005.

E. Dahl, D. Manthey, Y. Chen, H. J. Schwarz, Y. S. Chang et al., Molecular Cloning and Functional Expression of Mouse Connexin-30,a Gap Junction Gene Highly Expressed in Adult Brain and Skin, Journal of Biological Chemistry, vol.271, issue.30, pp.17903-17910, 1996.
DOI : 10.1074/jbc.271.30.17903

M. Esmaeili, M. Bonyadi, and M. Nejadkazem, Common mutation analysis of GJB2 and GJB6 genes in affected families with autosomal recessive non-syndromic hearing loss from Iran: Simultaneous detection of two common mutations (35delG/del(GJB6-D13S1830)) in the DFNB1-related deafness, International Journal of Pediatric Otorhinolaryngology, vol.71, issue.6, pp.869-873, 2007.
DOI : 10.1016/j.ijporl.2007.02.007

X. Estivill, P. Fortina, S. Surrey, R. Rabionet, S. Melchionda et al., Connexin-26 mutations in sporadic and inherited sensorineural deafness, The Lancet, vol.351, issue.9100, pp.394-398, 1998.
DOI : 10.1016/S0140-6736(97)11124-2

B. Gunther, A. Steiner, D. Nekahm-heis, K. Albegger, P. Zorowka et al., is not present in patients with non-syndromic hearing loss from Austria, Human Mutation, vol.22, issue.2, p.180, 2003.
DOI : 10.1002/humu.9167

H. Chaleshtori, M. , M. Zohour, M. , H. Rad et al., recessive and sporadic non syndromic hearing loss and the incidence of Cx26 mutations in a province of Iran, Autosomal Iran. J. Pub. Health, vol.35, pp.88-91, 2006.

E. Kalay, R. Caylan, H. Kremer, A. P. De-brouwer, and A. Karaguzel, GJB2 mutations in Turkish patients with ARNSHL: prevalence and two novel mutations, Hearing Research, vol.203, issue.1-2, pp.88-93
DOI : 10.1016/j.heares.2004.11.022

P. M. Kelley, E. Cohn, and W. J. Kimberling, required for normal auditory function, Connexin Brain Res. Rev, vol.26, issue.32, pp.184-188, 2000.

I. Lerer, M. Sagi, Z. Ben-neriah, T. Wang, H. Levi et al., A deletion mutation in GJB6 cooperating with a GJB2 mutation in trans in non-syndromic deafness: A novel founder mutation in Ashkenazi Jews, Human Mutation, vol.18, issue.5, p.460, 2001.
DOI : 10.1002/humu.1222

O. Posukh, N. Pallares-ruiz, V. Tadinova, L. Osipova, M. Claustres et al., First molecular screening of deafness in the Altai Republic population, BMC Medical Genetics, vol.5, issue.3, p.12, 2005.
DOI : 10.1097/01.GIM.0000066796.11916.94

R. Rabionet, L. Zelante, N. Lopez-bigas, L. D-'agruma, S. Melchionda et al., Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene, Human Genetics, vol.106, issue.1, pp.40-44, 2000.
DOI : 10.1007/s004390051007

A. Sadeghi, M. H. Sanati, F. Alasti, M. Hashemzadeh-chaleshtori, and M. Ataei, Mutation analysis of connexin 26 gene and del(GJB6-D13S1830) in patients with hereditary deafness from two provinces in Iran, Iran. J. Biotechnol, vol.3, pp.255-258, 2005.

I. Schrijver, Hereditary Non-Syndromic Sensorineural Hearing Loss, The Journal of Molecular Diagnostics, vol.6, issue.4, pp.275-284, 2004.
DOI : 10.1016/S1525-1578(10)60522-3
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1867482

L. Van-laer, P. Coucke, R. F. Mueller, G. Caethoven, K. Flothmann et al., A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment, Journal of Medical Genetics, vol.38, issue.8, pp.515-518, 2001.
DOI : 10.1136/jmg.38.8.515

V. K. Verselis, C. S. Ginter, and T. A. Bargiello, Opposite voltage gating polarities of two closely related onnexins, Nature, vol.368, issue.6469, pp.348-351, 1994.
DOI : 10.1038/368348a0