Mitochondrial complex deficiencies in a male with cardiomyopathy and 3‐methylglutaconic aciduria
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| Veröffentlicht in: | Journal of inherited metabolic disease 1995-03, Vol.18 (2), p.221-223 |
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| container_end_page | 223 |
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| container_issue | 2 |
| container_start_page | 221 |
| container_title | Journal of inherited metabolic disease |
| container_volume | 18 |
| creator | Besley, G. T. N. Lendon, M. Broadhead, D. M. Till, J. Heptinstall, L. E. Phillips, B. |
| description | |
| doi_str_mv | 10.1007/BF00711772 |
| format | Article |
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| fulltext | fulltext |
| identifier | ISSN: 0141-8955 |
| ispartof | Journal of inherited metabolic disease, 1995-03, Vol.18 (2), p.221-223 |
| issn | 0141-8955 1573-2665 |
| language | eng |
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| source | MEDLINE; SpringerLink Journals |
| subjects | 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 |
| title | Mitochondrial complex deficiencies in a male with cardiomyopathy and 3‐methylglutaconic aciduria |
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