Gly222Asp and Ser379Lys - Novel factor X gene mutations in severe FX deficiency - Greifswald registry of factor X congenital deficiency

被引：0
|
作者：
Herrmann, FH [1 ]
Wulff, K [1 ]
Lopaciuk, S [1 ]
Pollmann, H [1 ]
机构：
[1] Krankenhaus Lichtenberg, Klin Kinder & Jugendmed, Berlin, Germany
来源：
32ND HEMOPHILIA SYMPOSIUM | 2003年
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：49 / 57
页数：9
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