Compound heterozygosity for a novel mutation combined with G insertion in exon 13 causes severe factor XI deficiency in patients of Japanese origin.

被引：0
|
作者：
Ishikawa, N
Yasunaga, S
Otsubo, M
Takihara, Y
Sato, T
Kobayashi, M
机构：
[1] Hiroshima Univ, Grad Sch Biomed Sci, Hiroshima, Japan
[2] Res Inst Radiat Biol & Med, Hiroshima, Japan
来源：
BLOOD | 2005年 / 106卷 / 11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：
4087
引用
收藏
页码：102B / 102B
页数：1
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