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
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中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OC-TU-076
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收藏
页码:192 / 192
页数:1
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