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The connexin deafness homepage, 2009. http:\/\/davinci.crg.es\/deafness (Accessed April 16, 2009)."},{"key":"15","unstructured":"16. Camp GV, Willems PJ, Smith RJ. Nonsyndromic hearing impairment: Unparalleled heterogeneity. Am J Hum Genet. 1997; 60:758-764."},{"key":"16","doi-asserted-by":"crossref","unstructured":"17. Kelsell DP, Dunlop J, Stevens HP, Lench NJ, Liang JN, Parry G, Mueller RF, Leigh IM. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness. Nature. 1997; 387:80-83.","DOI":"10.1038\/387080a0"},{"key":"17","doi-asserted-by":"crossref","unstructured":"18. Marlin S, Feldmann D, Blons H, et al. GJB2 and GJB6 mutations: Genotypic and phenotypic correlations in a large cohort of hearing impaired patients. Arch Otolaryngol Head Neck Surg. 2005; 131:481-487.","DOI":"10.1001\/archotol.131.6.481"},{"key":"18","doi-asserted-by":"crossref","unstructured":"19. Snoeckx RL, Huygen PL, Feldmann D, et al. 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Update of the spectrum of GJB2 gene mutations in 152 Moroccan families with autosomal recessive nonsyndromic hearing loss. Eur J Med Genet. 2016, 59:325-329.","DOI":"10.1016\/j.ejmg.2016.05.002"},{"key":"26","unstructured":"27. Cui Q, Huang L, Ruan Y, Du Y, Zhao L, Yang J, Zhang W. The sequencing analyze of 915 newborn with GJB2 heterozygous mutation in Beijing. J Clin Otorhinolaryngol Head Neck Surg (China). 2015; 29:1164-1167."},{"key":"27","doi-asserted-by":"crossref","unstructured":"28. Wang QJ, Zhao YL, Rao SQ, Guo YF, He Y, Lan L, Yang WY, Zheng QY, Rubene RJ, Han DY, Shen Y. Newborn hearing concurrent gene screening can improve care for hearing loss: A study on 14913 Chinese newborns. Int J Pediatr Otorhinolaryngol. 2011; 75:535-542.","DOI":"10.1016\/j.ijporl.2011.01.016"},{"key":"28","doi-asserted-by":"crossref","unstructured":"29. Riahi Z, Hammami H, Ouragini H, et al. 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