Hermansky-Pudlak syndrome (HPS) as a genetically heterogeneous disease: Clinical, molecular, and cell biological aspects

被引：1
|
作者：
Gahl, WA
Shotelersuk, V
Brantly, M
Huizing, M
Dell'Angelica, EC
Bonifacino, JS
机构：
[1] NICHD, Heritable Disorders Branch, NIH, Bethesda, MD USA
[2] NHLBI, Pulm Crit Care Med Branch, NIH, Bethesda, MD 20892 USA
[3] NICHD, Cell Biol & Metab Branch, NIH, Bethesda, MD USA
来源：
PEDIATRIC RESEARCH | 1999年 / 45卷 / 04期
关键词：
D O I：
10.1203/00006450-199904020-00821
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
804
引用
收藏
页码：138A / 138A
页数：1
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