JIMD 2007
002-P The investigation of inherited metabolic disease in post mortem samples 019-P Enzymatic analysiss of MCAD, VLCAD, Glutaryl CoA dehydrogenase (GCDH), and isovaleryl CoA dehydrogenase (IVD) in lymphocytes with implications for neonatal screening 021-P More than one GCDH mutation causes glutaric aciduria type 1...