8037217

Source:http://linkedlifedata.com/resource/pubmed/id/8037217

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0012929, umls-concept:C0026882, umls-concept:C0028630, umls-concept:C0033551, umls-concept:C0237881, umls-concept:C0442996, umls-concept:C0750502, umls-concept:C0917796, umls-concept:C1521733, umls-concept:C1709450
pubmed:issue	2
pubmed:dateCreated	1994-8-15
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/8037217-8240356
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0370475
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/DNA, Mitochondrial, http://linkedlifedata.com/resource/pubmed/chemical/Deoxyribonucleases, Type II..., http://linkedlifedata.com/resource/pubmed/chemical/Electron Transport Complex IV, http://linkedlifedata.com/resource/pubmed/chemical/GGCC-specific type II...
pubmed:status	MEDLINE
pubmed:month	Aug
pubmed:issn	0002-9297
pubmed:author	pubmed-author:BrownM DMD, pubmed-author:ChenY SYS, pubmed-author:HuoponenKK, pubmed-author:LordM JMJ, pubmed-author:TorroniAA, pubmed-author:WallaceD CDC
pubmed:issnType	Print
pubmed:volume	55
pubmed:geneSymbol	COX III
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	410-2
pubmed:dateRevised	2009-11-18
pubmed:meshHeading	pubmed-meshheading:8037217-African Continental Ancestry Group, pubmed-meshheading:8037217-Blindness, pubmed-meshheading:8037217-DNA, Mitochondrial, pubmed-meshheading:8037217-Deoxyribonucleases, Type II Site-Specific, pubmed-meshheading:8037217-Electron Transport Complex IV, pubmed-meshheading:8037217-European Continental Ancestry Group, pubmed-meshheading:8037217-Humans, pubmed-meshheading:8037217-Mutation, pubmed-meshheading:8037217-Optic Atrophies, Hereditary
pubmed:year	1994
pubmed:articleTitle	Pathological significance of the mtDNA COX III mutation at nucleotide pair 9438 in Leber hereditary optic neuropathy.
pubmed:publicationType	Letter