| pubmed-article:15883259 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:15883259 | lifeskim:mentions | umls-concept:C0684336 | lld:lifeskim |
| pubmed-article:15883259 | lifeskim:mentions | umls-concept:C0917796 | lld:lifeskim |
| pubmed-article:15883259 | lifeskim:mentions | umls-concept:C0001480 | lld:lifeskim |
| pubmed-article:15883259 | lifeskim:mentions | umls-concept:C0205082 | lld:lifeskim |
| pubmed-article:15883259 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
| pubmed-article:15883259 | lifeskim:mentions | umls-concept:C0439855 | lld:lifeskim |
| pubmed-article:15883259 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
| pubmed-article:15883259 | pubmed:issue | 5 | lld:pubmed |
| pubmed-article:15883259 | pubmed:dateCreated | 2005-5-10 | lld:pubmed |
| pubmed-article:15883259 | pubmed:abstractText | Leber hereditary optic neuropathy (LHON) is a maternally inherited form of central vision loss associated with mitochondrial DNA point mutations that affect the ND subunits of complex I. | lld:pubmed |
| pubmed-article:15883259 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15883259 | pubmed:language | eng | lld:pubmed |
| pubmed-article:15883259 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15883259 | pubmed:citationSubset | AIM | lld:pubmed |
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| pubmed-article:15883259 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:15883259 | pubmed:month | May | lld:pubmed |
| pubmed-article:15883259 | pubmed:issn | 0003-9942 | lld:pubmed |
| pubmed-article:15883259 | pubmed:author | pubmed-author:CarelliValeri... | lld:pubmed |
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| pubmed-article:15883259 | pubmed:author | pubmed-author:LenazGiorgioG | lld:pubmed |
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| pubmed-article:15883259 | pubmed:author | pubmed-author:BaruzziAgosti... | lld:pubmed |
| pubmed-article:15883259 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:15883259 | pubmed:volume | 62 | lld:pubmed |
| pubmed-article:15883259 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:15883259 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:15883259 | pubmed:pagination | 730-6 | lld:pubmed |
| pubmed-article:15883259 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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| pubmed-article:15883259 | pubmed:meshHeading | pubmed-meshheading:15883259... | lld:pubmed |
| pubmed-article:15883259 | pubmed:year | 2005 | lld:pubmed |
| pubmed-article:15883259 | pubmed:articleTitle | Severe impairment of complex I-driven adenosine triphosphate synthesis in leber hereditary optic neuropathy cybrids. | lld:pubmed |
| pubmed-article:15883259 | pubmed:affiliation | Dipartimento di Biochimica, University of Bologna, Italy. | lld:pubmed |
| pubmed-article:15883259 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:15883259 | pubmed:publicationType | Comparative Study | lld:pubmed |
| pubmed-article:15883259 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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