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Abstract Glucose-6-phosphate dehydrogenase (G6PD) deficiency, one of the most common human genetic enzymopathies, is caused by over 160 different point mutations and contributes to the severity of many acute and chronic diseases associated with oxidative stress, including hemolytic anemia and bilirubin-induced neurological damage particularly in newborns

INCI Nomenclature:AHK-Cu (alanine/histidine/lysine)

No medical, therapeutic, or diagnostic claims are made or implied

Somatic mutations in MED12, which are implicated in modulating oxidative stress in uterine fibroids, are believed to be reliable biomarkers for these tumors [6,7]

N Engl J Med 2002