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

Author： Bhala A.  

Publisher： Oxford University Press

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.7, Iss.4, 1998-04, pp. : 619-627

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