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18625963
Source:
http://linkedlifedata.com/resource/pubmed/id/18625963
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pubmed-article:18625963
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pubmed-article:18625963
pubmed:issue
3
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pubmed-article:18625963
pubmed:dateCreated
2008-7-15
lld:pubmed
pubmed-article:18625963
pubmed:abstractText
To explore the involvement of M-type potassium channels KCNQ2, Q3, and Q5 in the pathogenesis of common idiopathic epilepsies.
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pubmed:language
eng
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AIM
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MEDLINE
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pubmed-article:18625963
pubmed:month
Jul
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pubmed-article:18625963
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1526-632X
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Electronic
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pubmed:day
15
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pubmed:volume
71
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NLM
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Y
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pubmed-article:18625963
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177-83
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pubmed-article:18625963
pubmed:year
2008
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pubmed-article:18625963
pubmed:articleTitle
KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes.
lld:pubmed
pubmed-article:18625963
pubmed:affiliation
Department of Pediatric Neurology, University of Giessen-Marburg, Feulgenstrasse 12, D-35385 Giessen, Germany. bernd.a.neubauer@paediat.med.uni-giessen.de
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pubmed-article:18625963
pubmed:publicationType
Journal Article
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pubmed-article:18625963
pubmed:publicationType
Comparative Study
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Research Support, Non-U.S. Gov't
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