Multiple carboxylase deficiency
Author:
Publisher
Elsevier BV
Subject
Biochemistry
Reference59 articles.
1. Biotin activation of carboxylase activity in cultured fibroblasts from a child with a combined carboxylase defect;Bartlett;Clin. chim. Acta,1978
2. Studies on cultured fibroblasts from patients with defects of biotin-dependent carboxylation;Bartlett;J. Inherit. Metab. Dis.,1981
3. A combined defect of three mitochondrial carboxylases presenting as biotin-responsive 3-methylcrotonyl glycinuria and 3-hydroxy-isovaleric aciduria;Bartlett;Clin chim. Acta,1980
4. Biotinidase deficiency; factors responsible for increased biotin requirement;Baumgartner;J. Inherit. Metab. Dis.,1985
5. Detection of biocytin in urine of children with congenital biotinidase deficiency;Bonjour;Int.J. Vitamin Nutr. Res.,1984
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