First Page | Document Content | |
---|---|---|
Date: 2009-02-03 16:52:41Fatty-acid metabolism disorder Mitochondrial trifunctional protein deficiency Newborn screening Fatty acid metabolism Very long-chain acyl-coenzyme A dehydrogenase deficiency Malonyl-CoA decarboxylase deficiency Health Medicine Rare diseases | Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)Add to Reading ListSource URL: health.mo.govDownload Document from Source WebsiteFile Size: 19,03 KBShare Document on Facebook |
DOCX DocumentDocID: 1wwhs - View Document | |
DOCX DocumentDocID: 1wv76 - View Document | |
PDF DocumentDocID: 1w4hN - View Document | |
-Application for Renewal of RDMM Catalyst Grants This application is to be used by the Network’s Scientific Advisory Committee (SAC) to determine as to whether to provide an additional year of funding ($DocID: 1vceh - View Document | |
MULTISYSTEMIC RARE DISEASESDocID: 1v3AN - View Document |