A study of a family with inherited disease of cardiac and skeletal muscle. Part II. Skeletal muscle morphology and mitochondrial oxidative phosphorylation

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dc.contributor.authorLochner, A.
dc.contributor.authorHewlett, R. H.
dc.contributor.authorO'Kennedy, A.
dc.contributor.authorVan der Walt, J. J.
dc.contributor.authorTiedt, F. A. C.
dc.contributor.authorHoffman, H.
dc.contributor.authorDe Graaf, A. S.
dc.contributor.authorPrzybojewski, J. Z.
dc.contributor.authorTorrington, M.
dc.date.accessioned2011-03-18T14:59:48Z
dc.date.available2011-03-18T14:59:48Z
dc.date.issued1981-03
dc.descriptionThe original publication is available at http://www.samj.org.za
dc.description.abstractSkeletal muscle morphology and mitochondrial oxidative phosphorylation capacity were examined in a family whose members showed varying combinations of mental subnormality, cardiomyopathy and muscle weakness. Light and electron microscopic findings suggested a neuropathic process, while tests of mitochondrial function indicated a state of tight coupling of oxidative phosphorylation, a feature in marked contrast to those in biochemical studies so far reported.en_ZA
dc.description.versionPublishers' version
dc.format.extent9 p. : ill.
dc.identifier.citationLochner A. et al. 1981. A study of a family with inherited disease of cardiac and skeletal muscle. II. Skeletal muscle morphology and mitochondrial oxidative phosphorylation. SA medical journal, 21 March: 453-461.
dc.identifier.issn2078-5135 (online) 0256-9574 (print)
dc.identifier.urihttp://hdl.handle.net/10019.1/8066
dc.language.isoen
dc.publisherHealth and Medical Publishing Group -- HMPG
dc.rights.holderThe authors
dc.subjectSkeletal muscle morphologyen_ZA
dc.subjectPhosphorylationen_ZA
dc.titleA study of a family with inherited disease of cardiac and skeletal muscle. Part II. Skeletal muscle morphology and mitochondrial oxidative phosphorylationen_ZA
dc.typeArticle
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