Mitochondrial complex deficiencies in a male with cardiomyopathy and 3‐methylglutaconic aciduria

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Bibliographische Detailangaben
Veröffentlicht in:	Journal of inherited metabolic disease 1995-03, Vol.18 (2), p.221-223
Hauptverfasser:	Besley, G. T. N., Lendon, M., Broadhead, D. M., Till, J., Heptinstall, L. E., Phillips, B.
Format:	Artikel
Sprache:	eng
Schlagworte:	Amino Acid Metabolism, Inborn Errors - complications Biological and medical sciences Cardiomyopathies - complications Child DNA Mutational Analysis Electron Transport Errors of metabolism Fatal Outcome Glutarates - urine Humans Male Medical sciences Metabolic diseases Miscellaneous hereditary metabolic disorders Mitochondria, Muscle - enzymology Mitochondrial Myopathies - complications Mitochondrial Myopathies - enzymology Mitochondrial Myopathies - genetics
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