Compound heterozygosity in four asymptomatic siblings with medium-chain acyl-CoA dehydrogenase deficiency

被引:4
作者
Albers, S
Levy, HL
Irons, M
Strauss, AW
Marsden, D
机构
[1] Childrens Hosp, Div Genet, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA
[3] Vanderbilt Univ, Dept Pediat, Nashville, TN USA
[4] New England Newborn Screening Program, Boston, MA USA
[5] Univ Massachusetts, Sch Med, Boston, MA 02125 USA
关键词
D O I
10.1023/A:1010533408635
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
[No abstract available]
引用
收藏
页码:417 / 418
页数:2
相关论文
共 3 条
[1]  
ANDRESEN BS, 1993, AM J HUM GENET, V53, P730
[2]  
Chace DH, 1997, CLIN CHEM, V43, P2106
[3]   Is the G985A allelic variant of medium-chain acyl-CoA dehydrogenase a risk factor for sudden infant death syndrome? A pooled analysis [J].
Wang, SS ;
Fernhoff, PM ;
Khoury, MJ .
PEDIATRICS, 2000, 105 (05) :1175-1176