Haemoglobin H hydrops fetalis syndrome associated with homozygosity for the α2-globin gene polyadenylation signal mutation AATAAA→AATA

被引:13
作者
Henderson, Shirley [1 ]
Chapple, Mary
Rugless, Michele
Fisher, Chris
Kinsey, Sally
Old, John
机构
[1] Oxford Radcliffe Hosp NHS Trust, Natl Haemoglobinopathy Reference Lab, Oxford, England
[2] Dewsbury & Dist Hosp, Dept Haematol, Dewsbury, W Yorkshire, England
[3] Weatherall Inst Mol Med, MRC, Mol Haematol Unit, Oxford, England
[4] St James Univ Hosp, Dept Haematol, Leeds LS9 7TF, W Yorkshire, England
关键词
alpha-thalassaemia; Hb H disease; Hb H hydrops fetalis; polyadenylation signal mutation;
D O I
10.1111/j.1365-2141.2006.06362.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:743 / 745
页数:5
相关论文
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