Clinical, biochemical, and mutational spectrum of peroxisomal acyl-coenzyme A oxidase deficiency. [electronic resource]
Producer: 20071002Description: 904-12 p. digitalISSN:- 1098-1004
- Acyl-CoA Oxidase
- Amino Acid Sequence
- Biomarkers -- analysis
- Cells, Cultured
- Cohort Studies
- DNA Mutational Analysis
- Fatty Acids -- analysis
- Fibroblasts -- chemistry
- Genotype
- Humans
- Isoenzymes -- genetics
- Lipid Metabolism, Inborn Errors -- genetics
- Molecular Sequence Data
- Mutation
- Oxidoreductases -- genetics
- Peroxisomal Disorders -- genetics
- Phenotype
- Sequence Homology, Amino Acid
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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