19733221

Source:http://linkedlifedata.com/resource/pubmed/id/19733221

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015576, umls-concept:C0026882, umls-concept:C0205251, umls-concept:C0206243, umls-concept:C0524899, umls-concept:C0814942, umls-concept:C0917796, umls-concept:C1537995
pubmed:issue	3
pubmed:dateCreated	2010-2-22
pubmed:abstractText	Leber's hereditary optic neuropathy (LHON) is a maternally inherited disorder. The purpose of this investigation is to understand the role of mitochondrial haplotypes in the development of LHON associated with ND6 T14484C mutation in Chinese families.
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/R01 DC007696-03, http://linkedlifedata.com/resource/pubmed/grant/R01DC05230, http://linkedlifedata.com/resource/pubmed/grant/R01DC07696
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pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0217513
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/DNA, Mitochondrial, http://linkedlifedata.com/resource/pubmed/chemical/MT-ND6 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/NADH Dehydrogenase
pubmed:status	MEDLINE
pubmed:month	Mar
pubmed:issn	0006-3002
pubmed:author	pubmed-author:GuanMin-XinMX, pubmed-author:IpN YNY, pubmed-author:LiangMinM, pubmed-author:LiuXiaolingX, pubmed-author:NgL SLS, pubmed-author:RodeM MMM, pubmed-author:SunYan-HongYH, pubmed-author:WeiQi-PingQP, pubmed-author:YangLiL, pubmed-author:YuanMeixiaM, pubmed-author:ZhangMinglianM, pubmed-author:ZhaoFuxinF, pubmed-author:ZhouXiangtianX
pubmed:copyrightInfo	Copyright (c) 2009 Elsevier B.V. All rights reserved.
pubmed:issnType	Print
pubmed:volume	1800
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	305-12
pubmed:dateRevised	2011-9-26
pubmed:meshHeading	pubmed-meshheading:19733221-Asian Continental Ancestry Group, pubmed-meshheading:19733221-China, pubmed-meshheading:19733221-DNA, Mitochondrial, pubmed-meshheading:19733221-Female, pubmed-meshheading:19733221-Humans, pubmed-meshheading:19733221-Male, pubmed-meshheading:19733221-Mutation, pubmed-meshheading:19733221-NADH Dehydrogenase, pubmed-meshheading:19733221-Optic Atrophy, Hereditary, Leber, pubmed-meshheading:19733221-Pedigree, pubmed-meshheading:19733221-Polymorphism, Single Nucleotide, pubmed-meshheading:19733221-Sequence Deletion, pubmed-meshheading:19733221-Visual Acuity, pubmed-meshheading:19733221-Visual Fields
pubmed:year	2010
pubmed:articleTitle	Low penetrance of Leber's hereditary optic neuropathy in ten Han Chinese families carrying the ND6 T11484C mutation.
pubmed:affiliation	School of Ophthalmology and Optometry, Wenzhou Medical College, Wenzhou, Zhejiang 325003, China. jqu@wzmc.net
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural