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Nutritional Therapy of the Deficits of Oxidation Mitochondrial of the Fatty Acids

Assistance Publique - Hôpitaux de Paris · 2006
ClinicalTrials.gov · Datasets · License: Public Domain · 2006
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longna
inborn errors of metabolism, fao disorders, long-chain fao enzyme defects, carnitine palmitoyltransferase 1 (cpt1),, carnitine-acylcarnitine translocase (cat),, carnitine palmitoyltransferase 2 (cpt2),, very-long chain acyl-coa dehydrogenase (vlcad),, l-3-hydroxy-acyl-coa dehydrogenase (lchad), or trifunctional protein (mtp)., interventional, na
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