c.426G>C mutation in ABO*A1.02 allele was associated with Aw phenotype

被引：1
|
作者：
Chen, Shu [1 ,2 ]
Hong, Xiaozhen [1 ,2 ]
Xu, Xianguo [1 ,2 ]
Ma, Kairong [1 ,2 ]
He, Ji [1 ,2 ]
Zhu, Faming [1 ,2 ]
机构：
[1] Blood Ctr Zhejiang Prov, Transfus Med Res Inst, JianYe Rd 789, Hangzhou 310052, Zhejiang, Peoples R China
[2] Key Lab Blood Safety Res Zhejiang Prov, Hangzhou, Zhejiang, Peoples R China
来源：
TRANSFUSION | 2019年 / 59卷 / 10期
关键词：
WEAK;
D O I：
10.1111/trf.15496
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：E4 / E5
页数：2
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