Microsoft Word - FINALDisordersDetectableTable42511 - Translocase - Document - PDFSEARCH.IO

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Date: 2014-08-13 12:31:27 Rare diseases Newborn screening Carnitine-acylcarnitine translocase deficiency Fatty-acid metabolism disorder Carnitine Phenylketonuria Glutaric aciduria type 1 Systemic primary carnitine deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Medicine Genetic genealogy		Microsoft Word - FINALDisordersDetectableTable42511 Add to Reading List Source URL: www.cdph.ca.gov Download Document from Source Website File Size: 66,50 KB Share Document on Facebook

	-0031 PEDIATRIC RESEARCH Copyright © 2011 International Pediatric Research Foundation, Inc. Vol. 70, No. 1, 2011 Printed in U.S.A. DocID: 1q0IJ - View Document
	There is a lot of research information available now on carnitine, that wasn’t around when we first started looking at carnitine supplementation for polios in 1994 and recording carnitine blood levels via PMH. Answers DocID: 1pSCZ - View Document
	Trimethylamine-N-oxide (TMAO) and cardiovascular outcome Manuel Ottiger, MD, Department of Internal Medicine Swiss MedLab Bern, Dietary-associated and intestinal microbiota-dependent DocID: 1pScc - View Document
	Supplement Facts BODY FORTRESS® KNOWS YOU DON’T CUT CORNERS IN TRAINING. THAT’S WHY WE DESIGNED A THERMOGENIC FORMULA THAT DOESN’T CUT CORNERS EITHER. SUPER ADVANCED SHRED IGNITER CONTAINS POWERFUL DOSAGES OF KEY DocID: 1pCC8 - View Document
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