Evaluation of branched-chain amino acid intake in children with maple syrup urine disease and methylmalonic aciduria.
Journal of inherited metabolic disease1990Parsons HG, Carter RJ, Unrath M, et al.
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MeSH
Amino Acid Metabolism, Inborn ErrorsAmino Acids, Branched-ChainAmmoniaBody WeightChild, PreschoolCreatinineDietary ProteinsFemaleFood, FormulatedGrowthHumansInfantInfant, NewbornIsoleucineLeucineMaleMalonatesMaple Syrup Urine DiseaseMethylmalonic AcidNutritional RequirementsValine