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Furthermore, a number of genetic mutations, such as LRRK2 , PRKN , DJ-1 , PINK1 , FBXO7 and ATP13A2 , in PD patients also provide clues of mitochondrial dysfunction in PD pathogenesis (see below)
2018, 10.1093/femsle/fny174
This problem affects cardiac electrical impulse conduction, leading to heart block
Your body continues to oxidize fat for energy just fine while you're supplementing with creatine
FukushiSMizutaniTSaijoMMatsuyamaSMiyajimaNTaguchiFet al
Dos Reis et al., 2024)
