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Description
As a result, primary coenzyme Q 10 deficiency is a clinically heterogeneous disorder that includes five major phenotypes: (i) severe infantile multi-systemic disease, (ii) encephalomyopathy, (iii) cerebellar ataxia, (iv) isolated myopathy, and (v) nephrotic syndrome
Sections of the atheroma with a deteriorated fibrous cap are subject to rupture (Figures 4 and 5) (168,169)

It detaches the L-carnitine and releases the long-chain fatty acid back to a mitochondrial Coenzyme A

Wann sollte ich kein L-Carnitin einnehmen

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[PMC free article: PMC3795453] [PubMed: 23939397] 704
