18625963

Source:http://linkedlifedata.com/resource/pubmed/id/18625963

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0014544, umls-concept:C0026882, umls-concept:C0039082, umls-concept:C0332240, umls-concept:C1416614, umls-concept:C1416615, umls-concept:C1880177
pubmed:issue	3
pubmed:dateCreated	2008-7-15
pubmed:abstractText	To explore the involvement of M-type potassium channels KCNQ2, Q3, and Q5 in the pathogenesis of common idiopathic epilepsies.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0401060
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/KCNQ2 Potassium Channel, http://linkedlifedata.com/resource/pubmed/chemical/KCNQ3 Potassium Channel
pubmed:status	MEDLINE
pubmed:month	Jul
pubmed:issn	1526-632X
pubmed:author	pubmed-author:EberhardFF, pubmed-author:Eeg-OlofssonOO, pubmed-author:FiedlerBB, pubmed-author:GarkischSS, pubmed-author:HahnAA, pubmed-author:HeinzingerJJ, pubmed-author:KurlemannGG, pubmed-author:MüllerUU, pubmed-author:MuhleHH, pubmed-author:NeubauerB ABA, pubmed-author:SanderTT, pubmed-author:StephanoSS, pubmed-author:WaldeggerSS
pubmed:issnType	Electronic
pubmed:day	15
pubmed:volume	71
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	177-83
pubmed:meshHeading	pubmed-meshheading:18625963-Adolescent, pubmed-meshheading:18625963-Adult, pubmed-meshheading:18625963-Animals, pubmed-meshheading:18625963-Case-Control Studies, pubmed-meshheading:18625963-Child, Preschool, pubmed-meshheading:18625963-DNA Mutational Analysis, pubmed-meshheading:18625963-Epilepsy, pubmed-meshheading:18625963-Female, pubmed-meshheading:18625963-Humans, pubmed-meshheading:18625963-Infant, Newborn, pubmed-meshheading:18625963-KCNQ2 Potassium Channel, pubmed-meshheading:18625963-KCNQ3 Potassium Channel, pubmed-meshheading:18625963-Male, pubmed-meshheading:18625963-Mutation, pubmed-meshheading:18625963-Mutation, Missense, pubmed-meshheading:18625963-Pedigree, pubmed-meshheading:18625963-Syndrome, pubmed-meshheading:18625963-Xenopus laevis
pubmed:year	2008
pubmed:articleTitle	KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes.
pubmed:affiliation	Department of Pediatric Neurology, University of Giessen-Marburg, Feulgenstrasse 12, D-35385 Giessen, Germany. bernd.a.neubauer@paediat.med.uni-giessen.de
pubmed:publicationType	Journal Article, Comparative Study, Research Support, Non-U.S. Gov't