12843334

Source:http://linkedlifedata.com/resource/pubmed/id/12843334

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0012929, umls-concept:C0026882, umls-concept:C0030705, umls-concept:C0376249, umls-concept:C0522498, umls-concept:C0750491, umls-concept:C0917796
pubmed:issue	7
pubmed:dateCreated	2003-7-4
pubmed:databankReference	http://linkedlifedata.com/resource/pubmed/xref/OMIM/535000
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985087R
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/DNA, Mitochondrial
pubmed:status	MEDLINE
pubmed:month	Jul
pubmed:issn	1468-6244
pubmed:author	pubmed-author:ChinneryP FPF, pubmed-author:JoblingM SMS, pubmed-author:TaylorR WRW, pubmed-author:TurnbullD MDM
pubmed:issnType	Electronic
pubmed:volume	40
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	e85
pubmed:dateRevised	2008-11-20
pubmed:meshHeading	pubmed-meshheading:12843334-DNA, Mitochondrial, pubmed-meshheading:12843334-DNA Mutational Analysis, pubmed-meshheading:12843334-Gene Frequency, pubmed-meshheading:12843334-Humans, pubmed-meshheading:12843334-Optic Atrophy, Hereditary, Leber, pubmed-meshheading:12843334-Point Mutation
pubmed:year	2003
pubmed:articleTitle	Frequency of rare mitochondrial DNA mutations in patients with suspected Leber's hereditary optic neuropathy.
pubmed:affiliation	Neurology, The Medical School, The University of Newcastle upon Tyne, UK.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't