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Date: 2007-06-25 16:36:03Health Solute carrier family Transport proteins Fatty acids Rare diseases Systemic primary carnitine deficiency Carnitine Fatty-acid metabolism disorder SLC22A5 Medicine Hepatology Biology | CARNITINE TRANSPORTER DEFICIENCY (CTD) REFERENCES (SYSTEMIC CARNITINE DEFICIENCY; CARNITINE DEFICIENCY, PRIMARY; CARNITINE UPTAKE DEFECT; CUD) 1. 2.Add to Reading ListSource URL: www.idph.state.ia.usDownload Document from Source WebsiteFile Size: 30,81 KBShare Document on Facebook |