15726411

Source:http://linkedlifedata.com/resource/pubmed/id/15726411

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0013421, umls-concept:C0037769, umls-concept:C0241888, umls-concept:C0596611, umls-concept:C1314792, umls-concept:C1425272
pubmed:issue	5
pubmed:dateCreated	2005-4-21
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7603873
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/ARX protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Homeodomain Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
pubmed:status	MEDLINE
pubmed:month	May
pubmed:issn	0340-6199
pubmed:author	pubmed-author:BoltshauserEugenE, pubmed-author:GrossClaudiaC, pubmed-author:HehrUteU, pubmed-author:SchmittBernhardB, pubmed-author:UyanikGoekhanG, pubmed-author:WinklerJürgenJ, pubmed-author:WohlrabGabrieleG
pubmed:issnType	Print
pubmed:volume	164
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	326-8
pubmed:meshHeading	pubmed-meshheading:15726411-Child, pubmed-meshheading:15726411-Child, Preschool, pubmed-meshheading:15726411-Dystonia, pubmed-meshheading:15726411-Homeodomain Proteins, pubmed-meshheading:15726411-Humans, pubmed-meshheading:15726411-Infant, pubmed-meshheading:15726411-Male, pubmed-meshheading:15726411-Mutation, pubmed-meshheading:15726411-Pedigree, pubmed-meshheading:15726411-Siblings, pubmed-meshheading:15726411-Spasms, Infantile, pubmed-meshheading:15726411-Transcription Factors
pubmed:year	2005
pubmed:articleTitle	Familial West syndrome and dystonia caused by an Aristaless related homeobox gene mutation.
pubmed:affiliation	Department of Neuropaediatrics and Neurophysiology, University Children's Hospital, Steinwiesstrasse 75, 8032 Zurich, Switzerland. gabriele.wohlrab@kispi.unizh.ch
pubmed:publicationType	Journal Article, Case Reports