Evidence for a common ancestral origin for the most frequent mutation responsible for surfactant protein B (SP-B) deficiency

被引：0
|
作者：
Nogee, L
Irrizary, K
Hamvas, A
Trusgnich, M
Cole, FS
机构：
[1] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
[2] Washington Univ, Sch Med, St Louis, MO USA
来源：
PEDIATRIC RESEARCH | 2000年 / 47卷 / 04期
关键词：
D O I：
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中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
2187
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页码：370A / 370A
页数：1
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