A Chinese family carrying novel mutations in SEC23B and HFE2, the genes responsible for congenital dyserythropoietic anaemia II (CDA II) and primary iron overload, respectively

被引：15
|
作者：
Liu, Gang [1 ]
Niu, Shiwen [1 ,2 ]
Dong, Ailian [1 ,3 ]
Cai, Hao [4 ,5 ]
Anderson, Gregory J. [6 ]
Han, Bing [4 ,5 ]
Nie, Guangjun [1 ]
机构：
[1] Natl Ctr Nanosci & Technol, CAS Key Lab Biol Effects Nanomat & Nanosafety, Beijing, Peoples R China
[2] Jilin Univ, Coll Pharmaceut Sci, Changchun 130023, Peoples R China
[3] Jilin Univ, Affiliated Hosp 1, Changchun 130023, Peoples R China
[4] Peking Union Med Coll, Beijing 100021, Peoples R China
[5] Chinese Acad Med Sci, Peking Union Med Coll Hosp, Dept Haematol, Beijing 100730, Peoples R China
[6] Queensland Inst Med Res, Iron Metab Lab, Brisbane, Qld 4006, Australia
来源：
BRITISH JOURNAL OF HAEMATOLOGY | 2012年 / 158卷 / 01期
关键词：
Novel mutation; SEC23B; HFE2; CDAII; Chinese family;
D O I：
10.1111/j.1365-2141.2012.09102.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：143 / 145
页数：3
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