Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:1.3.99.3 (
acyl-CoA dehydrogenase
)
1,425
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Mitochondrial fatty acids beta-oxidation is a repetitive process of four steps which provides the major source of energy for heart, liver and skeletal muscle. Several enzymes are involved in this spiral cycle. The
medium-chain acyl-CoA dehydrogenase
(
MCAD
), the short-chain acyl-CoA dehydrogenase (SCAD), the long-chain 3-hydroxy
acyl-CoA dehydrogenase
(LCHAD) and the carnitine-palmitoyl-CoA transferase II (CPT II) deficiency have been recognized as the most common inborn errors of metabolism and frequently reported in their association with sudden infant death (SID). The prevalent mutations in these genes need further investigation in different populations.
Beijing Da Xue Xue Bao Yi Xue
Ban
2006 Apr 18
PMID:[Study of the inborn errors of mitochondrial fatty acid beta-oxidation deficiency]. 1661 70
