15452324

Source:http://linkedlifedata.com/resource/pubmed/id/15452324

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0007758, umls-concept:C0014544, umls-concept:C0026882, umls-concept:C0231335, umls-concept:C0338484, umls-concept:C1456413
pubmed:issue	6
pubmed:dateCreated	2004-9-28
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0401060
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/CACNA1A protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Calcium Channels
pubmed:status	MEDLINE
pubmed:month	Sep
pubmed:issn	1526-632X
pubmed:author	pubmed-author:FerraroM JMJ, pubmed-author:FlinkRR, pubmed-author:FrantsR RRR, pubmed-author:GinjaarH BHB, pubmed-author:HabaTT, pubmed-author:KornE JEJ, pubmed-author:KumlienEE, pubmed-author:MelbergAA, pubmed-author:RaininkoRR, pubmed-author:VanmolkotK R JKR, pubmed-author:van den MaagdenbergA M J MAM
pubmed:issnType	Electronic
pubmed:day	28
pubmed:volume	63
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1136-7
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:15452324-Adult, pubmed-meshheading:15452324-Age of Onset, pubmed-meshheading:15452324-Amino Acid Substitution, pubmed-meshheading:15452324-Calcium Channels, pubmed-meshheading:15452324-Child, pubmed-meshheading:15452324-Child, Preschool, pubmed-meshheading:15452324-DNA Mutational Analysis, pubmed-meshheading:15452324-Disease Progression, pubmed-meshheading:15452324-Epilepsy, Complex Partial, pubmed-meshheading:15452324-Exons, pubmed-meshheading:15452324-Female, pubmed-meshheading:15452324-Haplotypes, pubmed-meshheading:15452324-Heterozygote, pubmed-meshheading:15452324-Humans, pubmed-meshheading:15452324-Male, pubmed-meshheading:15452324-Migraine with Aura, pubmed-meshheading:15452324-Migraine without Aura, pubmed-meshheading:15452324-Mutation, Missense, pubmed-meshheading:15452324-Pedigree, pubmed-meshheading:15452324-Point Mutation, pubmed-meshheading:15452324-Spinocerebellar Degenerations, pubmed-meshheading:15452324-Sweden
pubmed:year	2004
pubmed:articleTitle	Childhood epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutation.
pubmed:affiliation	Department of Neurology, Leiden University Medical Center, Leiden, The Netherlands.
pubmed:publicationType	Journal Article, Case Reports, Research Support, Non-U.S. Gov't