Hypoketonuric 3‐hydroxydicarboxylic aciduria in five patients with glycogen storage disease

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Bibliographische Detailangaben
Veröffentlicht in:	Journal of inherited metabolic disease 1997-07, Vol.20 (3), p.407-410
Hauptverfasser:	Mize, C. E., Waber, L. J., Anderson, T., Bennett, M. J.
Format:	Artikel
Sprache:	eng
Schlagworte:	Biological and medical sciences Carbohydrates (enzymatic deficiencies). Glycogenosis Cells, Cultured Child, Preschool Creatinine - urine Dicarboxylic Acids - urine Errors of metabolism Fatty Acids - metabolism Fatty Acids - urine Female Fibroblasts - metabolism Gas Chromatography-Mass Spectrometry Glycogen Storage Disease - urine Humans Infant Liver - enzymology Liver - pathology Male Medical sciences Metabolic diseases Oxidation-Reduction
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