Low prevalence of DFNB1 (connexin 26) mutations in British Pakistani children with non-syndromic sensorineural hearing loss | Archives of Disease in Childhood

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Low prevalence of DFNB1 (connexin 26) mutations in British Pakistani children with non-syndromic sensorineural hearing loss

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Cite this article as:: Yoong SY, Mavrogiannis LA, Wright J, et al

Low prevalence of DFNB1 (connexin 26) mutations in British Pakistani children with non-syndromic sensorineural hearing loss

Archives of Disease in Childhood 2011;96:798-803.