Functional characterisation of a novel splice mutation, c.7887+2T>A, associated with type 1 von Willebrand disease

被引：0

作者：

Cartwright, A. ^{[1
]}

Webster, S. J. ^{[1
]}

Jacobi, P. M. ^{[2
]}

Hickson, N. ^{[1
]}

Budde, U. ^{[3
]}

Peake, I. R. ^{[1
]}

Goodeve, A. C. ^{[1
]}

Haberichter, S. L. ^{[2
]}

Hampshire, D. J. ^{[1
]}

机构：

[1] Univ Sheffield, Dept Cardiovasc Sci, Sheffield, S Yorkshire, England

[2] BloodCtr Wisconsin, Blood Res Inst, Milwaukee, WI USA

[3] Medilys Hamburg, Hemostaseol Dept, Hamburg, Germany

来源：

JOURNAL OF THROMBOSIS AND HAEMOSTASIS | 2015年 / 13卷

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：

PO667-MON

引用

页码：505 / 505

页数：1

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Functional characterisation of a novel splice mutation, c.7887+2T&gt;A, associated with type 1 von Willebrand disease

Functional characterisation of a novel splice mutation, c.7887+2T>A, associated with type 1 von Willebrand disease