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

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