No abstract available
MeSH terms
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Disease Progression
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Electron Transport Complex I / deficiency
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Electron Transport Complex I / genetics
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Female
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Humans
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Infant
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Leukoencephalopathies / diagnosis*
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Leukoencephalopathies / etiology*
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Leukoencephalopathies / genetics
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Magnetic Resonance Imaging
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Mitochondrial Diseases / complications*
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Mitochondrial Diseases / diagnosis*
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Mitochondrial Diseases / genetics
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NADH Dehydrogenase / genetics
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Neuroimaging / methods
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Neurology / education
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Neurology / methods
Substances
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NDUFS1 protein, human
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NADH Dehydrogenase
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Electron Transport Complex I
Supplementary concepts
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Mitochondrial complex I deficiency