19167085

Source:http://linkedlifedata.com/resource/pubmed/id/19167085

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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:C1537992
pubmed:issue	3
pubmed:dateCreated	2009-3-6
pubmed:abstractText	To investigate the role of mitochondrial haplotypes in the development of Leber's hereditary optic neuropathy (LHON) associated with the ND4 G11778A mutation in Chinese families.
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/R01 DC005230-04, http://linkedlifedata.com/resource/pubmed/grant/R01 DC005230-05, http://linkedlifedata.com/resource/pubmed/grant/R01 DC007696-02, 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/7802443
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/DNA, Mitochondrial, http://linkedlifedata.com/resource/pubmed/chemical/NADH Dehydrogenase, http://linkedlifedata.com/resource/pubmed/chemical/NADH dehydrogenase subunit 4
pubmed:status	MEDLINE
pubmed:month	Mar
pubmed:issn	1549-4713
pubmed:author	pubmed-author:CaiWansiW, pubmed-author:GuanMin-XinMX, pubmed-author:NgL SLS, pubmed-author:RodeM MMM, pubmed-author:SunYan-HongYH, pubmed-author:WeiQi-PingQP, pubmed-author:WestConstance ECE, pubmed-author:YangLiL, pubmed-author:ZhangJuanjuanJ, pubmed-author:ZhaoFuxinF, pubmed-author:ZhouXiangtianX
pubmed:issnType	Electronic
pubmed:volume	116
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	558-564.e3
pubmed:dateRevised	2011-9-26
pubmed:meshHeading	pubmed-meshheading:19167085-Adolescent, pubmed-meshheading:19167085-Adult, pubmed-meshheading:19167085-Asian Continental Ancestry Group, pubmed-meshheading:19167085-Child, pubmed-meshheading:19167085-DNA, Mitochondrial, pubmed-meshheading:19167085-DNA Mutational Analysis, pubmed-meshheading:19167085-Evoked Potentials, Visual, pubmed-meshheading:19167085-Female, pubmed-meshheading:19167085-Humans, pubmed-meshheading:19167085-Male, pubmed-meshheading:19167085-Middle Aged, pubmed-meshheading:19167085-NADH Dehydrogenase, pubmed-meshheading:19167085-Optic Atrophy, Hereditary, Leber, pubmed-meshheading:19167085-Pedigree, pubmed-meshheading:19167085-Penetrance, pubmed-meshheading:19167085-Point Mutation, pubmed-meshheading:19167085-Polymerase Chain Reaction, pubmed-meshheading:19167085-Visual Acuity, pubmed-meshheading:19167085-Visual Fields, pubmed-meshheading:19167085-Young Adult
pubmed:year	2009
pubmed:articleTitle	Extremely low penetrance of Leber's hereditary optic neuropathy in 8 Han Chinese families carrying the ND4 G11778A mutation.
pubmed:affiliation	School of Ophthalmology and Optometry, Wenzhou Medical College, Wenzhou, Zhejiang, China.
pubmed:publicationType	Journal Article

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