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Autosomal recessive non-syndromic hearing loss in the Lebanese population: prevalence of the 30delG mutation and report of two novel mutations in the connexin 26 (GJB2) gene.

par Mustapha, M;Salem, N;Delague, V;Chouery, E;Ghassibeh, M;Rai, Myriam ;Loiselet, J;Petit, Christine ;Megarbane, Andre
Référence Journal of medical genetics, 38, 10, page (E36)
Publication Publié, 2001-10

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Titre:	Autosomal recessive non-syndromic hearing loss in the Lebanese population: prevalence of the 30delG mutation and report of two novel mutations in the connexin 26 (GJB2) gene.
Auteur:	Mustapha, M; Salem, N; Delague, V; Chouery, E; Ghassibeh, M; Rai, Myriam; Loiselet, J; Petit, Christine; Megarbane, Andre
Informations sur la publication:	Journal of medical genetics, 38, 10, page (E36)
Statut de publication:	Publié, 2001-10
Sujet CREF:	Sciences bio-médicales et agricoles
MeSH keywords:	Amino Acid Sequence
	Base Sequence
	Connexins -- chemistry -- genetics
	DNA Mutational Analysis
	Deafness -- epidemiology -- genetics
	Ethnic Groups -- genetics
	Exons -- genetics
	Female
	Genes, Recessive -- genetics
	Genetic Testing
	Heterozygote
	Humans
	Lebanon -- epidemiology
	Male
	Mutation -- genetics
	Prevalence
	Religion
	Sequence Deletion -- genetics
Note générale:	Letter
	Research Support, Non-U.S. Gov't
Langue:	Anglais
Identificateurs:	urn:issn:0022-2593
	info:pmid/11584050
	PMC1734738