Characterization of medium-chain acyl-CoA dehydrogenase (MCAD) with a point mutation associated with MCAD deficiency

Prog Clin Biol Res. 1992:375:473-8.

Authors

P Bross¹, T Jensen, F Kräutle, V Winter, B S Andresen, S Engst, L Bolund, S Kølvraa, S Ghisla, I Rasched, et al.

Affiliation

¹ Dept. of Clinical Chemistry, Arhus Kommunehospital, Denmark.

PMID: 1438390

No abstract available

Publication types

Research Support, Non-U.S. Gov't

MeSH terms

Acyl-CoA Dehydrogenase
Acyl-CoA Dehydrogenases / deficiency*
Acyl-CoA Dehydrogenases / genetics*
Animals
Cells, Cultured
Escherichia coli / genetics
Gene Expression Regulation, Bacterial / physiology*
Metabolism, Inborn Errors / enzymology
Metabolism, Inborn Errors / genetics*
Point Mutation / genetics*

Substances

Acyl-CoA Dehydrogenases
Acyl-CoA Dehydrogenase