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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
Rarely, allergic reactions may occur, leading to symptoms such as rashes, swelling, or difficulty breathing
10.1002/hep.23232 85
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