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Mahase E
Cai Y, Lei Y, Chen J, Cao L, Yang X, Zhang K, et al
Deficiency in MCAD is the most common defect observed in the process of mitochondrial -oxidation of fatty acids
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The effect of genetic polymorphism in response to body weight reduction in japanese patients with nonalcoholic fatty liver disease
It explains how PT-141 acts in the brain, its link to dopamine pathways and its connection with oxytocin
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