Van der Westhuizen, Francois H.; Smuts, Izelle; Honey, Engela M.; Louw, Roan; Schoonen, Maryke; Jonck, Lindi-Maryn; Dercksen, Marli(Elsevier, 2018-01)
Neonatal-onset multiple acyl-CoA dehydrogenase deficiency (MADD type I) is an autosomal recessive disorder of the electron transfer flavoprotein function characterized by a severe clinical and biochemical phenotype, including ...
