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Ramshankar M, Girirajan S, Dagan O, Shankar HMR, Jalvi R, Rangasayee R, Avraham KB, Anand A. Contribution of connexin26 (GJB2) mutations and founder effcet to non-syndromic hearing loss in India. J Med Genet. 2003; 40:e68.","DOI":"10.1136\/jmg.40.5.e68"},{"key":"6","doi-asserted-by":"crossref","unstructured":"6. Ghosh M, Vijaya R, Kabra M. Genetics of deafness in India. Indian J Pediatr. 2004; 71:531-533.","DOI":"10.1007\/BF02724296"},{"key":"7","doi-asserted-by":"crossref","unstructured":"7. Mani RS, Ganapathy A, Jalvi R, Srikumari Srisailapathy CR, Malhotra V, Chadha S, Agarwal A, Ramesh A, Rangasayee RR, Anand A. Functional consequences of novel connexin 26 mutations associated with hereditary hearing loss. Eur J Hum Genet. 2009; 17:502-509.","DOI":"10.1038\/ejhg.2008.179"},{"key":"8","doi-asserted-by":"crossref","unstructured":"8. Kemperman MH, Hoefsloot LH, Cremers CWRJ. Hearing loss and connexin 26. 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Denoyelle F, Weil D, Maw MA, <i>et al<\/i>. Prelingual deafness: High prevalence of a 30delG mutation in the connexin 26 gene. Hum Mol Genet. 1997; 6:2173-2177.","DOI":"10.1093\/hmg\/6.12.2173"},{"key":"17","doi-asserted-by":"crossref","unstructured":"17. Kelley PM, Harris DJ, Comer BC, Askew JW, Fowler T, Smith SD, Kimberling WJ. Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss. Am J Hum Genet. 1998; 62:792-799.","DOI":"10.1086\/301807"},{"key":"18","doi-asserted-by":"crossref","unstructured":"18. Yu X, Lin Y, Xu J, Che T, Li L, Yang T, Wu H. Molecular epidemiology of Chinese Han deaf patients with bi-allelic and mono-allelic GJB2 mutations. Orphanet J Rare Dis. 2020; 15:29.","DOI":"10.1186\/s13023-020-1311-2"},{"key":"19","doi-asserted-by":"crossref","unstructured":"19. Th\u00f6nnissen E, Rabionet R, Arbon\u00e8s ML, Estivill X, Willecke K, Ott T. 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