Type 2 Gaucher disease: An expanding phenotype

被引：34
作者：
Tayebi, N [1 ]
Stone, DL [1 ]
Sidransky, E [1 ]
机构：
[1] NIMH, Clin Neurosci Branch, NIH, Bethesda, MD 20892 USA
来源：
MOLECULAR GENETICS AND METABOLISM | 1999年 / 68卷 / 02期
关键词：
glucocerebrosidase deficiency; hydrops fetalis; congenital ichthyosis; genotype; lethal;
D O I：
10.1006/mgme.1999.2918
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：209 / 219
页数：11
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