Wolman disease due to homozygosity for a novel truncated variant of lysosomal acid lipase (351insA) associated with complete in situ acid lipase deficiency

被引：0
|
作者：
Seedorf, U
Heiko, W
Sandro, M
Ertan, M
Harald, F
Gerd, A
机构：
[1] UNIV MUNSTER,INST ARTERIOSKLEROSEFORSCH,D-4400 MUNSTER,GERMANY
[2] UNIV HEIDELBERG,HEIDELBERG,GERMANY
来源：
CIRCULATION | 1996年 / 94卷 / 08期
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：196 / 196
页数：2
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