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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
5
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pubmed:dateCreated |
2005-5-10
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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.
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pubmed:commentsCorrections |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
|
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0003-9942
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
62
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
730-6
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15883259-Adenosine Triphosphate,
pubmed-meshheading:15883259-Cells, Cultured,
pubmed-meshheading:15883259-Citric Acid,
pubmed-meshheading:15883259-DNA, Mitochondrial,
pubmed-meshheading:15883259-Electron Transport Complex I,
pubmed-meshheading:15883259-Fibroblasts,
pubmed-meshheading:15883259-Glutamates,
pubmed-meshheading:15883259-Humans,
pubmed-meshheading:15883259-Hybrid Cells,
pubmed-meshheading:15883259-Mutation,
pubmed-meshheading:15883259-Optic Atrophy, Hereditary, Leber,
pubmed-meshheading:15883259-Oxygen Consumption,
pubmed-meshheading:15883259-Succinic Acid
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pubmed:year |
2005
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pubmed:articleTitle |
Severe impairment of complex I-driven adenosine triphosphate synthesis in leber hereditary optic neuropathy cybrids.
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pubmed:affiliation |
Dipartimento di Biochimica, University of Bologna, Italy.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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