11584050

Source:http://linkedlifedata.com/resource/pubmed/id/11584050

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0017337, umls-concept:C0026882, umls-concept:C0032659, umls-concept:C0033105, umls-concept:C0163742, umls-concept:C0205314, umls-concept:C0441748, umls-concept:C0679622, umls-concept:C0684224, umls-concept:C1384666, umls-concept:C1415077, umls-concept:C1553356
pubmed:issue	10
pubmed:dateCreated	2001-10-3
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985087R
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Connexins, http://linkedlifedata.com/resource/pubmed/chemical/connexin 26
pubmed:status	MEDLINE
pubmed:month	Oct
pubmed:issn	1468-6244
pubmed:author	pubmed-author:ChoueryEE, pubmed-author:DelagueVV, pubmed-author:GhassibehMM, pubmed-author:LoiseletJJ, pubmed-author:MégarbanéAA, pubmed-author:MustaphaMM, pubmed-author:PetitCC, pubmed-author:RaeAA, pubmed-author:SalemNN
pubmed:issnType	Electronic
pubmed:volume	38
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	E36
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:11584050-Amino Acid Sequence, pubmed-meshheading:11584050-Base Sequence, pubmed-meshheading:11584050-Connexins, pubmed-meshheading:11584050-DNA Mutational Analysis, pubmed-meshheading:11584050-Deafness, pubmed-meshheading:11584050-Ethnic Groups, pubmed-meshheading:11584050-Exons, pubmed-meshheading:11584050-Female, pubmed-meshheading:11584050-Genes, Recessive, pubmed-meshheading:11584050-Genetic Testing, pubmed-meshheading:11584050-Heterozygote, pubmed-meshheading:11584050-Humans, pubmed-meshheading:11584050-Lebanon, pubmed-meshheading:11584050-Male, pubmed-meshheading:11584050-Mutation, pubmed-meshheading:11584050-Prevalence, pubmed-meshheading:11584050-Religion, pubmed-meshheading:11584050-Sequence Deletion
pubmed:year	2001
pubmed:articleTitle	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.
pubmed:publicationType	Letter, Research Support, Non-U.S. Gov't