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| pubmed-article:19733221 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:19733221 | pubmed:dateCreated | 2010-2-22 | lld:pubmed |
| pubmed-article:19733221 | 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. | lld:pubmed |
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| pubmed-article:19733221 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:19733221 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:19733221 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:19733221 | pubmed:month | Mar | lld:pubmed |
| pubmed-article:19733221 | pubmed:issn | 0006-3002 | lld:pubmed |
| pubmed-article:19733221 | pubmed:author | pubmed-author:RodeM MMM | lld:pubmed |
| pubmed-article:19733221 | pubmed:author | pubmed-author:IpN YNY | lld:pubmed |
| pubmed-article:19733221 | pubmed:author | pubmed-author:NgL SLS | lld:pubmed |
| pubmed-article:19733221 | pubmed:author | pubmed-author:YangLiL | lld:pubmed |
| pubmed-article:19733221 | pubmed:author | pubmed-author:LiangMinM | lld:pubmed |
| pubmed-article:19733221 | pubmed:author | pubmed-author:GuanMin-XinMX | lld:pubmed |
| pubmed-article:19733221 | pubmed:author | pubmed-author:ZhouXiangtian... | lld:pubmed |
| pubmed-article:19733221 | pubmed:author | pubmed-author:LiuXiaolingX | lld:pubmed |
| pubmed-article:19733221 | pubmed:author | pubmed-author:ZhaoFuxinF | lld:pubmed |
| pubmed-article:19733221 | pubmed:author | pubmed-author:SunYan-HongYH | lld:pubmed |
| pubmed-article:19733221 | pubmed:author | pubmed-author:WeiQi-PingQP | lld:pubmed |
| pubmed-article:19733221 | pubmed:author | pubmed-author:YuanMeixiaM | lld:pubmed |
| pubmed-article:19733221 | pubmed:author | pubmed-author:ZhangMinglian... | lld:pubmed |
| pubmed-article:19733221 | pubmed:copyrightInfo | Copyright (c) 2009 Elsevier B.V. All rights reserved. | lld:pubmed |
| pubmed-article:19733221 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:19733221 | pubmed:volume | 1800 | lld:pubmed |
| pubmed-article:19733221 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:19733221 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:19733221 | pubmed:pagination | 305-12 | lld:pubmed |
| pubmed-article:19733221 | pubmed:dateRevised | 2011-9-26 | lld:pubmed |
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| pubmed-article:19733221 | pubmed:year | 2010 | lld:pubmed |
| pubmed-article:19733221 | pubmed:articleTitle | Low penetrance of Leber's hereditary optic neuropathy in ten Han Chinese families carrying the ND6 T11484C mutation. | lld:pubmed |
| pubmed-article:19733221 | pubmed:affiliation | School of Ophthalmology and Optometry, Wenzhou Medical College, Wenzhou, Zhejiang 325003, China. jqu@wzmc.net | lld:pubmed |
| pubmed-article:19733221 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:19733221 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:19733221 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
| entrez-gene:6775063 | entrezgene:pubmed | pubmed-article:19733221 | lld:entrezgene |
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