Identification of four new mutations in the short-chain acyl-CoA dehydrogenase (SCAD) gene in two patients: one of the variant alleles, 511C–>T, is present at an unexpectedly high frequency in the general population, as was the case for 625G–>A, together conferring susceptibility to ethylmalonic aciduria. - Gregersen,N.; Winter,VS.; Corydon,MJ. (Hum Mol Genet, 1998)