reference/5136854

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publicationName	International Journal of Pediatric Otorhinolaryngology
startingPage	1633
bibliographicCitation	Nahili H, Ridal M, Boulouiz R, Abidi O, Imken L, Rouba H, Alami MN, Chafik A, Hassar M, Barakat A. Absence of GJB3 and GJB6 mutations in Moroccan familial and sporadic patients with autosomal recessive non-syndromic deafness. International Journal of Pediatric Otorhinolaryngology. 2008 Nov;72(11):1633–6. doi: 10.1016/j.ijporl.2008.07.015.
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date	200811
identifier	https://pubmed.ncbi.nlm.nih.gov/18809214 https://doi.org/10.1016/j.ijporl.2008.07.015
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Absence of GJB3 and GJB6 mutations in Moroccan familial and sporadic patients with autosomal recessive non-syndromic deafness
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