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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:dateCreated |
1989-1-26
|
| pubmed:abstractText |
In this paper selected data from 43 patients with histologically defined mitochondrial myopathies who have been investigated biochemically as previously described are presented. The defect was localized to NADH-ubiquinone oxidoreductase (complex I) in 22 cases and to ubiquinol-cytochrome c oxidoreductase (complex III) in a further 10. Two patients had defects of more than one respiratory enzyme complex and another had a deficiency of H+-ATPase. The lesion was not localized in two cases and in vitro mitochondrial studies were normal in five cases.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:issn |
0004-993X
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
24 Suppl 1
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
55-7
|
| pubmed:dateRevised |
2007-11-15
|
| pubmed:meshHeading |
pubmed-meshheading:2849394-Electron Transport Complex III,
pubmed-meshheading:2849394-Humans,
pubmed-meshheading:2849394-Mitochondria, Muscle,
pubmed-meshheading:2849394-Muscles,
pubmed-meshheading:2849394-Muscular Diseases,
pubmed-meshheading:2849394-NAD(P)H Dehydrogenase (Quinone),
pubmed-meshheading:2849394-Quinone Reductases
|
| pubmed:year |
1988
|
| pubmed:articleTitle |
Human mitochondrial respiratory chain deficiencies.
|
| pubmed:affiliation |
Institute of Neurology, National Hospital, London, England.
|
| pubmed:publicationType |
Journal Article,
Review,
Research Support, Non-U.S. Gov't
|