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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

The use of normal or genetically modified cells or cell components (e.g

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The cobalmin molecule can be combine with a cyanide molecule as in cynaocobalmin, a hydroxyl molecule as in hydroxycobalmin, methyl group as in methylcobalmin, or an adenosine molecule as in adenosylcobalmin