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• W2014183776 abstract "The recent finding that biotinidase deficiency is the primary biochemical defect in late-onset multiple carboxylase deficiency has stimulated new interest in the inherited disorders of biotin-dependent carboxylases. The clinical and biochemical features of biotinidase deficiency are discussed. We also speculate about two exciting areas currently being investigated: the localization of action of biotinidase, and the possible role of the enzyme as a binding or carrier protein for biotin." @default.
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• W2014183776 date "1985-03-01" @default.
• W2014183776 modified "2023-10-03" @default.
• W2014183776 title "Biotinidase deficiency: A novel vitamin recycling defect" @default.
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• W2014183776 doi "https://doi.org/10.1007/bf01800660" @default.
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