No abstract available
MeSH terms
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Cardiomyopathies / etiology
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DNA, Mitochondrial / genetics
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Diagnosis, Differential
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Electron Transport Complex III / deficiency*
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Humans
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Mitochondrial Myopathies / etiology
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Multiple Organ Failure / etiology
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Point Mutation
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Prognosis
Substances
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DNA, Mitochondrial
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Electron Transport Complex III