Very-long-chain polyunsaturated fatty acids accumulate in phosphatidylcholine of fibroblasts from patients with Zellweger syndrome and acyl-CoA oxidase1 deficiency. [electronic resource]
Producer: 20140528Description: 610-9 p. digitalISSN:- 0006-3002
- Acyl Coenzyme A -- deficiency
- Adrenoleukodystrophy -- genetics
- Animals
- Cells, Cultured
- Cricetinae
- Fatty Acids, Unsaturated -- metabolism
- Fibroblasts -- metabolism
- Humans
- Oxidation-Reduction
- Peroxisomal Disorders -- metabolism
- Peroxisomes -- metabolism
- Phosphatidylcholines -- metabolism
- Zellweger Syndrome -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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