Is the G985A allelic variant of medium-chain acyl-CoA dehydrogenase a risk factor for sudden infant death syndrome? A pooled analysis

被引：8

作者：

Wang, SS ^{[1
]}

Fernhoff, PM

Khoury, MJ

机构：

[1] Ctr Dis Control & Prevent, Natl Ctr Environm Hlth, Off Genet & Dis Prevent, Atlanta, GA 30341 USA

[2] Emory Univ, Dept Pediat, Div Med Genet, Atlanta, GA 30322 USA

来源：

PEDIATRICS | 2000年 / 105卷 / 05期

关键词：

D O I：

10.1542/peds.105.5.1175

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：1175 / 1176

页数：2

共 5 条

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[2] Retrospective biochemical screening of fatty acid oxidation disorders in postmortem livers of 418 cases of sudden death in the first year of life [J].

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Buck, EA ;

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Rinaldo, P .

JOURNAL OF PEDIATRICS, 1998, 132 (06) :924-933

[3] IS GENOTYPING USEFUL FOR THE SCREENING OF MEDIUM-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY IN FRANCE [J].

GED, C ;

ELSEBAI, H ;

DEVERNEUIL, H ;

PARROTROULEAU, F .

JOURNAL OF INHERITED METABOLIC DISEASE, 1995, 18 (02) :253-256

[4] FREQUENCY OF MEDIUM-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY G-985-MUTATION IN SUDDEN-INFANT-DEATH-SYNDROME [J].

MILLER, ME ;

BROOKS, JG ;

FORBES, N ;

INSEL, R .

PEDIATRIC RESEARCH, 1992, 31 (04) :305-307

[5]

Wang SS, 1999, GENET MED, V1, P332

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