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...
03 marzo, 2023
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