Microsoft Word - FAOD.doc - Mitochondrial diseases - Document - PDFSEARCH.IO

First Page		Document Content
Date: 2007-05-01 14:47:24 Fatty-acid metabolism disorder Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Short-chain acyl-coenzyme A dehydrogenase deficiency Fatty acid metabolism Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Mitochondrial trifunctional protein deficiency Newborn screening Lipid Health Medicine Rare diseases		Microsoft Word - FAOD.doc Add to Reading List Source URL: health.tn.gov Download Document from Source Website File Size: 46,17 KB Share Document on Facebook

	Int. J. BiosciInternational Journal of Biosciences (IJB) ISSN: PrintOnline) Vol. 1, No. 6, p, 2011 DocID: 17AqU - View Document
	Medium chain acyl-CoA Dehydrogenase Deficiency (MCADD) DocID: HZG0 - View Document
	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. Patient DocID: HuOH - View Document
	Microsoft Word - mso31.doc DocID: HkpM - View Document
	Microsoft Word - FAOD.doc DocID: HahR - View Document