Molecular characterization of medium-chain acyl-CoA dehydrogenase deficiency causing sudden death

Prog Clin Biol Res. 1992:375:463-72.

Authors

D P Kelly¹, A J Whelan, D E Hale, P Rinaldo, S L Rutledge, Z Zhang, A W Strauss

Affiliation

¹ Washington University, St. Louis, MO 63110.

PMID: 1438388

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
Base Sequence
Catalysis
Cells, Cultured
Child, Preschool
Gene Expression Regulation, Enzymologic / physiology*
Humans
Infant
Metabolism, Inborn Errors / complications
Metabolism, Inborn Errors / enzymology
Metabolism, Inborn Errors / genetics*
Molecular Sequence Data
Mutation / genetics
Sudden Infant Death / etiology*

Substances

Acyl-CoA Dehydrogenases
Acyl-CoA Dehydrogenase