Homozygosity mapping reveals founder SEC23B-Y462C mutations in Indian congenital dyserythropoietic anemia type II

被引：10
|
作者：
Singleton, B. [1 ]
Bansal, D. [2 ]
Varma, N. [3 ]
Das, R. [3 ]
Naseem, S. [3 ]
Saikia, U. N. [4 ]
Malhotra, P. [5 ]
Varma, S. [5 ]
Marwaha, R. K. [2 ]
King, M. -J. [6 ]
Ahmed, M. [7 ]
机构：
[1] NHSBT, Bristol Inst Transfus Sci, Bristol Inst Transfus Sci, Bristol, Avon, England
[2] PGIMER, Adv Paediat Ctr, Pediat Haematol Oncol Unit, Chandigarh, India
[3] PGIMER, Dept Haematol, Chandigarh, India
[4] PGIMER, Dept Histopathol, Chandigarh, India
[5] PGIMER, Dept Internal Med, Chandigarh, India
[6] NHSBT, Int Blood Grp Reference Lab, Membrane Biochem, Bristol, Avon, England
[7] Kings Coll Hosp London, Leukaemia Genom & Bone Marrow Failure Grp, Dept Haematol Med, London SE5 9NU, England
来源：
CLINICAL GENETICS | 2015年 / 88卷 / 02期
关键词：
GENE ACCOUNT; POPULATION;
D O I：
10.1111/cge.12527
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：195 / 197
页数：3
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