Title : Clinical, biochemical, and mutational spectrum of peroxisomal acyl-coenzyme A oxidase deficiency.

Pub. Date : 2007 Sep

PMID : 17458872






1 Functional Relationships(s)
Download
Sentence
Compound Name
Protein Name
Organism
1 Peroxisomal acyl-coenzyme A (acyl-CoA) oxidase deficiency is an autosomal recessive inborn error of peroxisomal fatty acid oxidation due to a deficiency of straight-chain acyl-CoA oxidase (SCOX). Fatty Acids acyl-CoA oxidase 1 Homo sapiens