The mutational spectrum in very long-chain acyl-CoA dehydrogenase deficiency

被引：34
|
作者：
Andresen, BS
VianeySaban, C
Bross, P
Divry, P
Roe, CR
Nada, MA
Knudsen, I
Gregersen, N
机构：
[1] AARHUS UNIV HOSP,CTR MED MOL BIOL,DK-8000 AARHUS,DENMARK
[2] SKEJBY SYGEHUS,FAC HLTH SCI,DK-8200 AARHUS,DENMARK
[3] HOP DEBROUSSE,UNITE ETUD MALAD METAB,LYON,FRANCE
[4] BAYLOR UNIV,MED CTR,INST METAB DIS,DALLAS,TX
来源：
JOURNAL OF INHERITED METABOLIC DISEASE | 1996年 / 19卷 / 02期
关键词：
D O I：
10.1007/BF01799421
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：169 / 172
页数：4
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