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Date: 2014-08-08 20:00:05Chemistry Dietary supplements Quaternary ammonium compounds Carnitine Systemic primary carnitine deficiency Hypoglycemia Carnitine palmitoyltransferase I deficiency Carnitine-acylcarnitine translocase deficiency Medicine Health Hepatology | PARENT FACT SHEET DISORDER Carnitine uptake defect (CUD) CAUSE CUD occurs when an enzyme, called “carnitine transporter” (CT), is either missing or not working properly.Add to Reading ListSource URL: chfs.ky.govDownload Document from Source WebsiteFile Size: 35,35 KBShare Document on Facebook |
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Carnitine/Acylcarnitine Translocase Deficiency (CACT) A fatty acid oxidation disorder What is it? Carnitine/Acylcarnitine Translocase Deficiency (also known as CACT) is an inherited fatty acid oxidation disorder. PatientDocID: HuOH - View Document | |
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