Cytochrome c Oxidase: Organ-Specific Isoenzymes and Deficiencies View Full Text


Ontology type: schema:Chapter     


Chapter Info

DATE

1988

AUTHORS

K. M. C. Sinjorgo , T. B. M. Hakvoort , A. O. Muijsers , A. W. Schram , J. M. Tager

ABSTRACT

Ever since the first report of Luft et al. (1962), considerable information has become available on inherited metabolic diseases originating from defects in mitochondria. Apart from defects in the import of substrates, in the carboxylic acid cycle, and in fatty acid oxidation, many dysfunctions have been described in the mitochondrial respiratory chain and ATP synthase (Morgan-Hughes, 1980). In the present study, we focused on defects of cytochrome c oxidase (E.C. 1.9.3.1), the terminal component of the mitochondrial respiratory chain. More... »

PAGES

202-204

Book

TITLE

Studies in Inherited Metabolic Disease

ISBN

978-94-010-7059-1
978-94-009-1259-5

Author Affiliations

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/978-94-009-1259-5_31

DOI

http://dx.doi.org/10.1007/978-94-009-1259-5_31

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1012202713


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