1. Biotinresponsive organic aciduria: multiple carboxylase defects and complementation studies with propionic acidemia in cultured fibroblasts;Saunders;J. Clin. Invest.,1979
2. A combined defect of three mitochondrial carboxylases presenting as biotin-responsive 3-methylcrotonylglycinuria and 3-hydroxyisovaleric aciduria;Bartlett;Clin. Chim. Acta,1980
3. Wolf, B., Hsia, Y.E., Sweetman, L., Feldman, G., Boychuk, R.B., Bart, R.D., Crowell, D.H., Di Mauro, R.M. and Nyhan, W.L. Multiple carboxylase deficiency: clinical and biochemical improvement following neonatal biotin treatment. Pediatr., in press
4. Fatty-acid responsive alopecia in multiple carboxylase deficiency;Munnich;Lancet,1980
5. Biochemical characterization of multiple carboxylase deficiency: heterogeneity within a complementation group;Feldman;Am. J. Hum. Genet.,1980