Neonatal screening for biotinidase deficiency: An update
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01799736
Reference7 articles.
1. Craft, D. V., Cross, N. H., Chandramouli, N. and Wood, H. G. Purification of biotinidase from human plasma and its activity on biotinyl peptides.Biochemistry 24 (1985) 2471–2476
2. Heard, G. S., Secor McVoy, J. R. and Wolf, B. A screening method for biotinidase deficiency in newborns.Clin. Chem. 30 (1984) 125–127
3. Pispa, J. Animal biotinidase.Ann. Med. Exp. Biol. Fenn. 43 Suppl. 5 (1965) 5–39
4. Wolf, B., Grier, R. E., Allen, R. J., Goodman, S. I. and Kien, C. L. Biotinidase deficiency: the enzymatic defect in late-onset multiple carboxylase deficiency.Clin. Chim. Acta 131 (1983a) 272–281
5. Wolf, B., Grier, R. E., Allen, R. J., Goodman, S. I., Kien, C. L., Parker, W. D., Howell, D. M. and Hurst, D. L. Phenotypic variation in biotinidase deficiency.J. Pediatr. 103 (1983b) 233–237
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