An inherited disorder that prevents carnitine from normally attaching to long-chain fatty acids that is used to make energy in the mitochondria. Mutations in the CPT1A gene severely reduce or eliminate the activity of this enzyme.
An inherited disorder that prevents carnitine from normally attaching to long-chain fatty acids that is used to make energy in the mitochondria. Mutations in the CPT1A gene severely reduce or eliminate the activity of this enzyme.
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