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Parakh S, Atkin JD
Eur J Pharm Sci 114:6473
Activating de novo mutations in NFE2L2 encoding NRF2 cause a multisystem disorder
24-Hydroxylase Deficiency Genetic loss of the catabolic effects of 24-hydroxylase (CYP24A1) causes high calcitriol, mild hypercalcemia, and nephrolithiasis in non-pregnant adults, which may be asymptomatic (203)
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37 This regeneration of GSH from GSSG is one of the roles of melatonin in reducing or preventing free radical damage
