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doi: 10.1016/j.freeradbiomed.2020.10.010

A novel homozygous KLHL3 mutation as a cause of autosomal recessive pseudohypoaldosteronism type II diagnosed late in life

Autoantibodies to a 68/48 kDa protein in chronic fatigue syndrome and primary fibromyalgia: a possible marker for hypersomnia and cognitive disorders

This reduced form combines with free radicals like superoxide, hydroxyl, hypochlorous acid, peroxyl, and singlet oxygen to exert its antioxidant potential [136]

(1) Bains J

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