Functional characterisation of 13-bp deletion mutation (-1255 del) in the VWF gene promoter causing type 1 von willebrand disease

被引：0
|
作者：
Othman, M. [1 ]
Chirinian, Y. [1 ]
Brown, C. [1 ]
Notely, C. [1 ]
Buckley, S. [2 ]
Waddington, S. N. [3 ]
Baker, A. H. [4 ]
Lillicrap, D. [1 ]
机构：
[1] Queens Univ, Pathol & Mol Med, Kingston, ON, Canada
[2] Imperial Coll, Hematol, London, England
[3] Imperial Coll, Hematol, London, ON, Canada
[4] Univ Glasgow, Cardiovasc Res Ctr, Glasgow, Scotland
来源：
JOURNAL OF THROMBOSIS AND HAEMOSTASIS | 2009年 / 7卷
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D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
OC-TU-076
引用
收藏
页码：192 / 192
页数：1
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