16021496

Source:http://linkedlifedata.com/resource/pubmed/id/16021496

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0013867, umls-concept:C0026882, umls-concept:C0029124, umls-concept:C0030705, umls-concept:C0205160, umls-concept:C0205314, umls-concept:C0332281, umls-concept:C0679622, umls-concept:C1417953
pubmed:issue	2
pubmed:dateCreated	2006-2-23
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8205248
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/GTP Phosphohydrolases, http://linkedlifedata.com/resource/pubmed/chemical/OPA1 protein, human
pubmed:status	MEDLINE
pubmed:month	Feb
pubmed:issn	0721-832X
pubmed:author	pubmed-author:MiyakeYozoY, pubmed-author:NakamuraMakotoM
pubmed:issnType	Print
pubmed:volume	244
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	274-5
pubmed:meshHeading	pubmed-meshheading:16021496-Electroretinography, pubmed-meshheading:16021496-Female, pubmed-meshheading:16021496-GTP Phosphohydrolases, pubmed-meshheading:16021496-Humans, pubmed-meshheading:16021496-Male, pubmed-meshheading:16021496-Middle Aged, pubmed-meshheading:16021496-Mutation, pubmed-meshheading:16021496-Optic Atrophy, Autosomal Dominant
pubmed:year	2006
pubmed:articleTitle	Optic atrophy and negative electroretinogram in a patient associated with a novel OPA1 mutation.
pubmed:publicationType	Letter, Research Support, Non-U.S. Gov't