Author:
Briones P.,Ribes A.,Vilaseca M. A.,Rodríguez-Valcárcel G.,Thuy L. P.,Sweetman L.
Subject
Genetics(clinical),Genetics
Reference3 articles.
1. Bartlett, K., Ghneim, H. K., Stirk, H.-J. and Wastell, H. Enzyme studies in biotin-responsive disorders.J. Inher. Metab. Dis. 8 Suppl. 1 (1985) 45–52
2. Burri, B. J., Sweetman, L. and Nyhan, W. L. Heterogeneity of holocarboxylase synthetase in patients with biotin-responsive multiple carboxylase deficiency.Am. J. Hum. Genet. 37 (1985) 326–337
3. Sherwood, W. G., Saunders, M., Robinson, B. H., Brewster, T. and Gravel, R. A. Lactic acidosis in biotin responsive multiple carboxylase deficiency caused by holocarboxylase synthetase deficiency of early and late onset.J. Pediatr. 101 (1982) 546–550
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