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MGAT2 inhibitor decreases liver fibrosis and inflammation in murine NASH models and reduces body weight in human adults with obesity

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Many of the disorders that result from defects in mitochondrial biogenesis and/or function have multiple genetic causes such that manifestation can result from maternal inheritance, X-linked inheritance, autosomal recessive inheritance, or autosomal dominant inheritance, or they can be the result of sporadic somatic mutation

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