2760006

Source:http://linkedlifedata.com/resource/pubmed/id/2760006

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0018523
pubmed:issue	8
pubmed:dateCreated	1989-9-20
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/2760006-2914882
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7801243
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Aug
pubmed:issn	0160-6689
pubmed:author	pubmed-author:MillerM BMB
pubmed:issnType	Print
pubmed:volume	50
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	309
pubmed:dateRevised	2007-11-15
pubmed:meshHeading	pubmed-meshheading:2760006-Basal Ganglia Diseases, pubmed-meshheading:2760006-Female, pubmed-meshheading:2760006-Genes, Dominant, pubmed-meshheading:2760006-Genes, Recessive, pubmed-meshheading:2760006-Genotype, pubmed-meshheading:2760006-Humans, pubmed-meshheading:2760006-Male, pubmed-meshheading:2760006-Pantothenate Kinase-Associated Neurodegeneration
pubmed:year	1989
pubmed:articleTitle	Hallervorden-Spatz disease.
pubmed:publicationType	Letter, Comment