Severe factor VII deficiency caused by compound heterozygous mutation (Tyr68Cys and newly 1-bp deletion)

被引：0
|
作者：
Shinozawa, K. [1 ]
Hanabusa, H.
Kinai, E.
Suzuki, T. [2 ]
Amano, K. [1 ,2 ]
Fukutake, K. [1 ,2 ]
机构：
[1] Tokyo Med Univ, Dept Mol Genet Coagulat Disorders, Tokyo, Japan
[2] Tokyo Med Univ, Dept Lab Med, Tokyo, Japan
来源：
HAEMOPHILIA | 2008年 / 14卷
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D O I：
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中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
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页码：69 / 69
页数：1
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