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MESH1 is a cytosolic NADPH phosphatase that regulates ferroptosis

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In fact, several recent studies that have conducted genome wide searches for common genetic defects across large samples of ASD children have only identified rare de novo mutations, thereby pointing to acquired mutations and/or mutations secondary to errors in DNA maintenance rather than inherited genetic syndromes (11, 12)

Vorburger SA, Pataer A, Swisher SG , Hunt KK

Cellular Compartmentalization, Glutathione Transport and Its Relevance in Some Pathologies

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