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Date: 2007-06-25 16:36:03Biology Carnitine palmitoyltransferase I Carnitine CPT2 Fatty-acid metabolism disorder Myoglobinuria Fatty acid metabolism Carnitine-acylcarnitine translocase deficiency Inborn error of lipid metabolism Medicine Hepatology Health | Microsoft Word - cpt2_refAdd to Reading ListSource URL: www.idph.state.ia.usDownload Document from Source WebsiteFile Size: 36,46 KBShare Document on Facebook |
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Example of VLCAD Protocol To Whom It May Concern: Re: (Name of child) Date of Birth: _____________ is a __ year old boy with very long chain acyl-CoA dehydrogenase (VLCAD) deficiency, an inborn error of mitochondrial fatDocID: D3ZI - View Document | |
Microsoft Word - cpt2_refDocID: y1VR - View Document |