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62Isolated (biotin-resistant) 3-methylcrotonyl-CoA carboxylase deficiency: four sibs devoid of pathology, Journal of Inherited Metabolic Disease Screening for defects of branched-chain amino acid metabolism, European Journal of Pediatrics Variable clinical presentation in three patients with 3-methylglutaconyl-coenzyme A hydratase deficiency, Journal of Inherited Metabolic Disease Condensation of carboxylic esters with ethyl ethynyl ether, Bulletin of the Academy of Sciences of the USSR, Division of chemical science Barth Syndrome: An X-linked Cardiomyopathy with a Novel Mutation, The Indian Journal of Pediatrics 3-methylglutaconyl-coenzyme-A hydratase deficiency: A new case, Journal of Inherited Metabolic Disease Incidence of 3-hydroxy-3-methylglutaryl-coenzyme A lyase (HL) deficiency in Brazil, South America, Journal of Inherited Metabolic Disease