11971066

Source:http://linkedlifedata.com/resource/pubmed/id/11971066

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0007758, umls-concept:C0026882, umls-concept:C0206243, umls-concept:C0338484, umls-concept:C0868928, umls-concept:C1456413, umls-concept:C1556094
pubmed:issue	5
pubmed:dateCreated	2002-4-23
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985191R
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/CACNA1A protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Calcium Channels
pubmed:status	MEDLINE
pubmed:month	May
pubmed:issn	0022-3050
pubmed:author	pubmed-author:HozumiII, pubmed-author:IgarashiSS, pubmed-author:KawachiII, pubmed-author:KimuraTT, pubmed-author:OnoderaOO, pubmed-author:SaitoMM, pubmed-author:TakahashiTT, pubmed-author:TakanoHH, pubmed-author:TsujiSS
pubmed:issnType	Print
pubmed:volume	72
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	676-7
pubmed:dateRevised	2008-11-20
pubmed:meshHeading	pubmed-meshheading:11971066-Adult, pubmed-meshheading:11971066-Aged, pubmed-meshheading:11971066-Brain, pubmed-meshheading:11971066-Calcium Channels, pubmed-meshheading:11971066-Cerebellar Ataxia, pubmed-meshheading:11971066-Chromosomes, Human, Pair 19, pubmed-meshheading:11971066-DNA Mutational Analysis, pubmed-meshheading:11971066-Female, pubmed-meshheading:11971066-Genotype, pubmed-meshheading:11971066-Hemiplegia, pubmed-meshheading:11971066-Humans, pubmed-meshheading:11971066-Japan, pubmed-meshheading:11971066-Magnetic Resonance Imaging, pubmed-meshheading:11971066-Male, pubmed-meshheading:11971066-Middle Aged, pubmed-meshheading:11971066-Migraine Disorders, pubmed-meshheading:11971066-Phenotype, pubmed-meshheading:11971066-Point Mutation, pubmed-meshheading:11971066-Tomography, Emission-Computed, Single-Photon
pubmed:year	2002
pubmed:articleTitle	Japanese cases of familial hemiplegic migraine with cerebellar ataxia carrying a T666M mutation in the CACNA1A gene.
pubmed:publicationType	Letter, Case Reports