A novel R1205C candidate type 1 von Willebrand disease mutation in the same codon as type 2 'Vincenza' in two affected siblings of a Scottish family

被引：0
|
作者：
Enayat, MS
Chalmers, E
Williams, MD
Hill, FGH
机构：
[1] Birmingham Childrens Hosp NHS Trust, Dept Haematol, Mol Haemostasis Lab, Birmingham, W Midlands, England
[2] Royal Hosp Sick Children, Dept Haematol, Glasgow G3 8SJ, Lanark, Scotland
来源：
BRITISH JOURNAL OF HAEMATOLOGY | 2004年 / 125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：
160
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页码：50 / 50
页数：1
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