Why screen newborns for profound and partial biotinidase deficiency?
Author:
Funder
Safra Research Fund
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference50 articles.
1. Deficient biotinidase activity in late-onset multiple carboxylase deficiency;Wolf;N. Engl. J. Med.,1983
2. Biotinidase deficiency: the enzymatic defect in late-onset multiple carboxylase deficiency;Wolf;Clin. Chim. Acta,1983
3. A screening method for biotinidase deficiency in newborns;Heard;Clin. Chem.,1984
4. Neonatal screening for biotinidase deficiency: results of a 1-year pilot study;Heard;J. Pediatr.,1986
5. Worldwide survey of neonatal screening for biotinidase deficiency;Wolf;J. Inherit. Metab. Dis.,1991
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