18279427

Source:http://linkedlifedata.com/resource/pubmed/id/18279427

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015576, umls-concept:C0025362, umls-concept:C0026882, umls-concept:C0332307, umls-concept:C0338484, umls-concept:C0740279, umls-concept:C1456413, umls-concept:C2827424
pubmed:issue	4
pubmed:dateCreated	2008-3-4
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8200710
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	Apr
pubmed:issn	1468-2982
pubmed:author	pubmed-author:BoheMM, pubmed-author:DichgansMM, pubmed-author:FreilingerTT, pubmed-author:KnoblauchHH, pubmed-author:Müller-MyhsokBB, pubmed-author:WegenerBB
pubmed:issnType	Electronic
pubmed:volume	28
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	403-7
pubmed:dateRevised	2011-11-17
pubmed:meshHeading	pubmed-meshheading:18279427-Adult, pubmed-meshheading:18279427-Atrophy, pubmed-meshheading:18279427-Calcium Channels, pubmed-meshheading:18279427-Cerebellar Diseases, pubmed-meshheading:18279427-Family Health, pubmed-meshheading:18279427-Humans, pubmed-meshheading:18279427-Intellectual Disability, pubmed-meshheading:18279427-Middle Aged, pubmed-meshheading:18279427-Migraine with Aura, pubmed-meshheading:18279427-Phenotype, pubmed-meshheading:18279427-Point Mutation
pubmed:year	2008
pubmed:articleTitle	Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation.
pubmed:affiliation	Department of Neurology, Ludwig-Maximilians-Universität München, Klinikum Grosshadern, Munich, Germany. tobias.freilinger@med.uni-muenchen.de
pubmed:publicationType	Journal Article, Case Reports