共 141 条
[3]
Adam BW, 2000, CLIN CHEM, V46, P126
[4]
Isolated 2-methylbutyrylglycinuria caused by short/branched-chain acyl-CoA dehydrogenase deficiency: Identification of a new enzyme defect, resolution of its molecular basis, and evidence for distinct acyl-CoA dehydrogenases in isoleucine and valine metabolism
[J].
AMERICAN JOURNAL OF HUMAN GENETICS,
2000, 67 (05)
:1095-1103
[5]
Medium-chain Acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-Based prospective screening of newborns differ from those observed in patients with clinical symptoms: Identification and characterization of a new, prevalent mutation that results in mild MCAD deficiency
[J].
AMERICAN JOURNAL OF HUMAN GENETICS,
2001, 68 (06)
:1408-1418
[6]
Bellisario R, 2000, CLIN CHEM, V46, P1422
[8]
BENNETT M J, 1991, Pediatric Pathology, V11, P365
[10]
Bennett MJ, 2001, CLIN CHEM, V47, P1145

