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35Studies on cultured fibroblasts from patients with defects of biotin-dependent carboxylation, Journal of Inherited Metabolic Disease A case of biotin-responsive 3-methylcrotonylglycin- and 3-hydroxyisovaleric aciduria, European Journal of Pediatrics 3-Hydroxyisovalerylcarnitine in 3-methylcrotonyl-CoA carboxylase deficiency, Journal of Inherited Metabolic Disease Isolated (biotin-resistant) 3-methylcrotonyl-CoA carboxylase deficiency: four sibs devoid of pathology, Journal of Inherited Metabolic Disease Glycine andl-carnitine therapy in 3-methylcrotonyl-CoA carboxylase deficiency, Journal of Inherited Metabolic Disease Late-infantile 3-methylcrotonyl-CoA carboxylase deficiency presenting as global developmental delay, Journal of Inherited Metabolic Disease Biotin Disorders, Physician's Guide to the Diagnosis, Treatment, and Follow-Up of Inherited Metabolic Diseases Isolated Biotin-Resistant 3-Methylcrotonyl-CoA Carboxylase Deficiency, Inborn Metabolic Diseases Organic Aciduria in Late-onset Biotin-responsive Multiple Carboxylase Deficiency, Inherited Disorders of Vitamins and Cofactors Biotin-responsive 3-Methylcrotonylglycinuria with Biotinidase Deficiency, Inherited Disorders of Vitamins and Cofactors