17562939

Source:http://linkedlifedata.com/resource/pubmed/id/17562939

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Subject	Predicate	Object	Context
pubmed-article:17562939	rdf:type	pubmed:Citation	lld:pubmed
pubmed-article:17562939	lifeskim:mentions	umls-concept:C0917796	lld:lifeskim
pubmed-article:17562939	lifeskim:mentions	umls-concept:C1838879	lld:lifeskim
pubmed-article:17562939	lifeskim:mentions	umls-concept:C0026882	lld:lifeskim
pubmed-article:17562939	lifeskim:mentions	umls-concept:C1424660	lld:lifeskim
pubmed-article:17562939	lifeskim:mentions	umls-concept:C0678227	lld:lifeskim
pubmed-article:17562939	pubmed:issue	6	lld:pubmed
pubmed-article:17562939	pubmed:dateCreated	2007-6-12	lld:pubmed
pubmed-article:17562939	pubmed:abstractText	To report a novel mutation that is associated with Leber hereditary optic neuropathy (LHON) within the same family affected by spastic dystonia.	lld:pubmed
pubmed-article:17562939	pubmed:language	eng	lld:pubmed
pubmed-article:17562939	pubmed:journal	http://linkedlifedata.com/r...	lld:pubmed
pubmed-article:17562939	pubmed:citationSubset	AIM	lld:pubmed
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pubmed-article:17562939	pubmed:status	MEDLINE	lld:pubmed
pubmed-article:17562939	pubmed:month	Jun	lld:pubmed
pubmed-article:17562939	pubmed:issn	0003-9942	lld:pubmed
pubmed-article:17562939	pubmed:author	pubmed-author:Maat-KievitAA	lld:pubmed
pubmed-article:17562939	pubmed:author	pubmed-author:SpruijtLiesbe...	lld:pubmed
pubmed-article:17562939	pubmed:author	pubmed-author:SluiterWimW	lld:pubmed
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pubmed-article:17562939	pubmed:author	pubmed-author:HendrickxAlex...	lld:pubmed
pubmed-article:17562939	pubmed:author	pubmed-author:Schoonderwoer...	lld:pubmed
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pubmed-article:17562939	pubmed:issnType	Print	lld:pubmed
pubmed-article:17562939	pubmed:volume	64	lld:pubmed
pubmed-article:17562939	pubmed:owner	NLM	lld:pubmed
pubmed-article:17562939	pubmed:authorsComplete	Y	lld:pubmed
pubmed-article:17562939	pubmed:pagination	890-3	lld:pubmed
pubmed-article:17562939	pubmed:dateRevised	2007-8-10	lld:pubmed
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pubmed-article:17562939	pubmed:meshHeading	pubmed-meshheading:17562939...	lld:pubmed
pubmed-article:17562939	pubmed:year	2007	lld:pubmed
pubmed-article:17562939	pubmed:articleTitle	A MELAS-associated ND1 mutation causing leber hereditary optic neuropathy and spastic dystonia.	lld:pubmed
pubmed-article:17562939	pubmed:affiliation	Department of Genetics and Cell Biology, University of Maastricht, PO Box 616, 6200 MD Maastricht, the Netherlands.	lld:pubmed
pubmed-article:17562939	pubmed:publicationType	Journal Article	lld:pubmed
pubmed-article:17562939	pubmed:publicationType	Case Reports	lld:pubmed
pubmed-article:17562939	pubmed:publicationType	Research Support, Non-U.S. Gov't	lld:pubmed
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