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

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.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.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.format.extent9 p. : ill.
dc.language.isoen
dc.publisherHealth and Medical Publishing Group -- HMPG
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
dc.description.versionPublishers' version
dc.rights.holderThe authors


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