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Heymsfield SB, Greenberg AS, Fujioka K, et al

These studies indicate the potential of utilizing the de novo pathway, a less extensively studied pathway, as a therapeutic strategy for metabolic diseases Barth syndrome is a rare disease caused by mutations in the tafazzin gene encoding for cardiolipin (CL), a phospholipid specific for the mitochondria 303

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Instead, it acts as a signaling tool, helping your body coordinate how and where to respond to stress or injury

QuZ and XW provided logistics support for both in vivo and in vitro experiments