P.E1549K: a new mutation responsible of von willebrand disease type 2M

被引:0
|
作者
Woods, A., I [1 ]
Sanchez-Luceros, A. [1 ]
Kempfer, A. C. [1 ]
Bermejo, E., I [1 ]
Calderazzo, J. C. [1 ]
Blanco, A. N. [1 ]
Meschengieser, S. S. [1 ]
Lazzari, M. A. [1 ]
机构
[1] Inst Invest Hematol, Buenos Aires, DF, Argentina
关键词
missense mutation; p.E1549K; VWD 2M variant;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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页码:102 / 102
页数:1
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