Two forms of biotin-responsive multiple carboxylase deficiency
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF02263587
Reference7 articles.
1. Baker, H., Frank, O., Matovich, V. B., Pasher, I., Aaronson, S., Hutner, S. H. and Sobotka, H. A new assay method for biotin in blood, serum, urine and tissues.Anal. Biochem. 3 (1962) 31–39
2. Cowan, M. J., Wara, D. W., Packman, S., Ammann, A. J., Yoshino, M., Sweetman, L. and Nyhan, W. L. Multiple biotin-dependent carboxylase deficiencies associated with defects in T-cell and B-cell immunity.Lancet 2 (1979) 115–118
3. Gompertz, D., Draffan, G. H., Watts, J. L. and Hull, D. Biotin-responsive β-methylcrotonylglycinuria.Lancet 2 (1971) 22–24
4. Roth, K., Cohn, R., Yandrasitz, J.et al. Beta-methylcrotonic aciduria associated with lactic acidosis.J. Pediatr. 88 (1976) 229–235
5. Saunders, M., Sweetman, L., Robinson, B., Roth, K., Cohn, R. and Gravel, R. A. Biotin-response organicaciduria: multiple carboxylase defects and complementation studies with propionic acidemia in cultured fibroblasts.J. Clin. Invest. 64 (1979) 1695–1702
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