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10.1016/j.xphs.2019.04.022 2 BainS
CL Tests Reveal the Best Huperzine A Supplements for Memory
Indeed, mitochondrial impairment caused by mutations in genes linked to familial PD, together with data from human post-mortem tissue indicate that impaired mitochondrial function, increased oxidative stress and deficient anti-oxidant capacity are common pathological mechanisms implicated in the etiology of both familial and sporadic PD cases (Dauer and Przedborski, 2003
3B, Table S5)
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