21112924

Source:http://linkedlifedata.com/resource/pubmed/id/21112924

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0019425, umls-concept:C0026882, umls-concept:C0221061, umls-concept:C1417953
pubmed:issue	Pt 4
pubmed:dateCreated	2011-4-4
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/21112924-20157015
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0372537
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/GTP Phosphohydrolases, http://linkedlifedata.com/resource/pubmed/chemical/OPA1 protein, human
pubmed:status	MEDLINE
pubmed:month	Apr
pubmed:issn	1460-2156
pubmed:author	pubmed-author:Amati-BonneauPatriziaP, pubmed-author:BonneauDominiqueD, pubmed-author:BriceAlexisA, pubmed-author:BrissaudEtienneE, pubmed-author:DurrAlexandraA, pubmed-author:LayetAntoineA, pubmed-author:LayetValérieV, pubmed-author:MarelliCeciliaC, pubmed-author:ReynierPascalP, pubmed-author:StevaninGiovanniG
pubmed:issnType	Electronic
pubmed:volume	134
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	e169; author reply e170
pubmed:dateRevised	2011-11-17
pubmed:meshHeading	pubmed-meshheading:21112924-Ataxia, pubmed-meshheading:21112924-GTP Phosphohydrolases, pubmed-meshheading:21112924-Hearing Loss, pubmed-meshheading:21112924-Humans, pubmed-meshheading:21112924-Intellectual Disability, pubmed-meshheading:21112924-Mutation, pubmed-meshheading:21112924-Optic Atrophy, pubmed-meshheading:21112924-Spasm
pubmed:year	2011
pubmed:articleTitle	Heterozygous OPA1 mutations in Behr syndrome.
pubmed:publicationType	Letter, Comment, Research Support, Non-U.S. Gov't