An altered redox balance and increased genetic instability characterize primary fibroblasts derived from xeroderma pigmentosum group A patients
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Increased levels and different types of intracellular radical species as well as an altered glutathione redox state characterize XP-A human cells when compared to normal.

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A more glycolytic metabolism and higher ATP levels are associated with alteration of mitochondrial morphology and response to mitochondrial toxicants when XPA is defective.

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XP-A human cells show increased spontaneous micronuclei frequency, a hallmark of cancer risk.

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