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These claims should be grounded in rigorous study designs, including clinical trials when available, and that regulatory status can vary by jurisdiction

Our recent work adds loss of mitochondrial MAT1, an important regulator of mitochondrial function, as another mechanism[19]

It protects cells from oxidative stress and supports detoxification

Conclusion Considering the strong evolutionary conservation of ironsulfur clusters and its biosynthetic pathway throughout eukaryotes, it is not surprising that deficiencies in this synthesis pathway can cause severe impairment of cellular functioning and affect the viability of affected organisms