Studies on phytanoyl-CoA 2-hydroxylase and synthesis of phytanoyl-Coenzyme A

Author:

Kershaw Nadia J,Mukherji Mridul,MacKinnon Colin H,Claridge Timothy D.W,Odell Barbara,Wierzbicki Anthony S,Lloyd Matthew D,Schofield Christopher J

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference26 articles.

1. Wanders, R. J. A.; Jakobs, C.; Skjelda, O. M. Refsum's disease. In The Metabolic and Molecular Basis of Inherited Disease; Scriver, C. R., Beaudet, A. L., Sly, W. S., Valle, D., Childs, B., Kinzler, K. W., Vogelstein, B., Eds.; McGraw Hill: New York, 2001; pp 3303–3321.

2. Refsum's disease: characterization of the enzyme defect in cell culture

3. Identification of PAHX, a Refsum disease gene

4. Human Very-Long-Chain Acyl-CoA Synthetase: Cloning, Topography, and Relevance to Branched-Chain Fatty Acid Metabolism

5. Refsum disease is caused by mutations in the phytanoyl–CoA hydroxylase gene

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