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![]() Date: 2015-02-26 15:37:45Rare diseases Fatty-acid metabolism disorder Very long-chain acyl-coenzyme A dehydrogenase deficiency Glutaric aciduria type 1 Carnitine Biotinidase deficiency Biotin Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Genetic genealogy Medical genetics | Add to Reading List |
![]() | POSTER SESSIONS The LIPID MAPS meeting features two poster sessions with 44 posters. Of these, twelve were selected for lightning talks (see program) by the review committee, consisting of Susan A. Henry, Alfred H. MerriDocID: 19Ufx - View Document |
![]() | What is Carnitine ? Nelson LS Tang, MBChB, FRCPA Associate Professor Department of Chemical Pathology The Chinese University of Hong KongDocID: 13Fs6 - View Document |
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![]() | Disorders and Reference RangesDocID: KTuv - View Document |