Fatal cardiomyopathy associated with 3‐hydroxy‐3‐methylglutaryl‐CoA lyase deficiency

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Bibliographische Detailangaben
Veröffentlicht in:	Journal of inherited metabolic disease 1994-05, Vol.17 (3), p.291-294
Hauptverfasser:	Gibson, K. M., Cassidy, S. B., Seaver, L. H., Wanders, R. J. A., Kennaway, N. G., Mitchell, G. A., Spark, R. P.
Format:	Artikel
Sprache:	eng
Schlagworte:	Amino Acid Metabolism, Inborn Errors - complications Amino Acid Metabolism, Inborn Errors - pathology Biological and medical sciences Cardiomyopathy, Dilated - enzymology Cardiomyopathy, Dilated - etiology Cardiomyopathy, Dilated - pathology Errors of metabolism Fatal Outcome Gas Chromatography-Mass Spectrometry Heart Ventricles - pathology Humans Infant Male Medical sciences Metabolic diseases Miscellaneous hereditary metabolic disorders Oxo-Acid-Lyases - deficiency
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