Hypoketonuric 3-hydroxydicarboxylic aciduria in five patients with glycogen storage disease.

Authors :: Mize CE
Waber LJ
Anderson T
Bennett MJ
Source :: Journal of inherited metabolic disease [J Inherit Metab Dis] 1997 Jul; Vol. 20 (3), pp. 407-10.
Publication Year :: 1997

Subjects :: Cells, Cultured
Child, Preschool
Creatinine urine
Fatty Acids urine
Female
Fibroblasts metabolism
Gas Chromatography-Mass Spectrometry
Humans
Infant
Liver enzymology
Liver pathology
Male
Oxidation-Reduction
Dicarboxylic Acids urine
Fatty Acids metabolism
Glycogen Storage Disease urine

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