Fatty acid transport in multiple carboxylase deficiency fibroblasts
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01799574
Reference13 articles.
1. Bloch, K. and Vance, D. Control mechanisms in the synthesis of saturated fatty acids.Ann. Rev. Biochem. 46 (1977) 263–298
2. Burri, B., Sweetman, L. and Nyhan, W. Mutant holocarboxylase synthetase: evidence for the enzyme defect in early infantile biotin-responsive multiple carboxylase deficiency.J. Clin. Invest. 68 (1981) 1491–1495
3. Feldman, G. and Wolf, B. Deficient acetyl-CoA carboxylase activity in multiple carboxylase deficiency.Clin. Chim. Acta 111 (1981) 147–151
4. Gonzalez-Rios, M. C., Whitney, S., Williams, M., Elias, P. and Packman, S. Lipid metabolism in biotin-responsive multiple deficiency.J. Inher. Metab. Dis. 8 (1985) 184–186
5. Kim, K. H. Control of acetyl-CoA carboxylase by covalent modification.Mol. Cell Biochem. 28 (1979) 28–43
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