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The presence of complex V subcomplexes in patients with defective intramitochondrial protein translation
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Two novel mitochondrial DNA mutations in muscle tissue of a patient with limb-girdle myopathy
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Detection of complex III deficient patients using a novel activity staining method in the BN-page gel
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Visualizing oxidative phosphorylation defects in skeletal muscle of patients with mitochondrial tRNA gene mutations using immunohistochemistry
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Infantile presentation of the mitochondrial A8344G mutation.
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Complex V subcomplexes detected by BN PAGE are a sign of a defective intramitochondrial protein translation
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Complex V subcomplexes suggestive of a defective intramitochondrial protein translation.
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Complex V subcomplexes suggestive of a defective intramitochondrial protein translation
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A novel mitochondrial tRNA Asn mutation causing multi-organ failure
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Diagnostics in mitochondrial diseases: the need of collaboration between clinician and research laboratories.