19380705

Source:http://linkedlifedata.com/resource/pubmed/id/19380705

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0012655, umls-concept:C0013421, umls-concept:C0205419, umls-concept:C0241888, umls-concept:C0868928, umls-concept:C1521761, umls-concept:C1540039
pubmed:issue	16
pubmed:dateCreated	2009-4-21
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0401060
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Molecular Chaperones, http://linkedlifedata.com/resource/pubmed/chemical/TOR1A protein, human
pubmed:status	MEDLINE
pubmed:month	Apr
pubmed:issn	1526-632X
pubmed:author	pubmed-author:AltenmüllerEE, pubmed-author:BrüggemannNN, pubmed-author:HagenahJJ, pubmed-author:JabuschH CHC, pubmed-author:KönigI RIR, pubmed-author:KleinCC, pubmed-author:KochKK, pubmed-author:LohmannKK, pubmed-author:MünchauAA, pubmed-author:RakovicAA, pubmed-author:SchmidtAA, pubmed-author:SiebnerHH, pubmed-author:ZieglerAA
pubmed:issnType	Electronic
pubmed:day	21
pubmed:volume	72
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1441-3
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:19380705-Adult, pubmed-meshheading:19380705-Aged, pubmed-meshheading:19380705-Blepharospasm, pubmed-meshheading:19380705-DNA Mutational Analysis, pubmed-meshheading:19380705-Dystonia, pubmed-meshheading:19380705-Dystonic Disorders, pubmed-meshheading:19380705-Family Health, pubmed-meshheading:19380705-Female, pubmed-meshheading:19380705-Gene Frequency, pubmed-meshheading:19380705-Genetic Predisposition to Disease, pubmed-meshheading:19380705-Genetic Testing, pubmed-meshheading:19380705-Genetic Variation, pubmed-meshheading:19380705-Genotype, pubmed-meshheading:19380705-Germany, pubmed-meshheading:19380705-Humans, pubmed-meshheading:19380705-Male, pubmed-meshheading:19380705-Middle Aged, pubmed-meshheading:19380705-Molecular Chaperones, pubmed-meshheading:19380705-Penetrance, pubmed-meshheading:19380705-Polymorphism, Genetic, pubmed-meshheading:19380705-Torticollis
pubmed:year	2009
pubmed:articleTitle	The D216H variant in the DYT1 gene: a susceptibility factor for dystonia in familial cases?
pubmed:affiliation	Department of Neurology, University of Lübeck, Germany.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't