Identification of a novel A allele with initiator codon variant (c.2T > A) in the ABO gene associated with weak A phenotype

被引:0
|
作者
Ying, Yanling [1 ,2 ]
Hong, Xiaozhen [1 ,2 ]
Zhang, Jingjing [1 ,2 ]
Huang, Xinyu [1 ,2 ]
Zhu, Faming [1 ,2 ,3 ]
机构
[1] Transfus Res Inst, Blood Ctr Zhejiang Prov, Hangzhou, Peoples R China
[2] Key Lab Blood Safety Res Zhejiang Prov, Hangzhou, Peoples R China
[3] Blood Ctr Zhejiang Prov, JianYe Rd 789, Hangzhou 310052, Zhejiang, Peoples R China
关键词
blood group genomics; immunohematology (RBC serology; blood groups);
D O I
10.1111/trf.17295
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:E23 / E24
页数:2
相关论文
共 50 条
  • [31] Identification of a novel variant CYP2C9 allele in Chinese
    Si, DY
    Guo, YJ
    Zhang, YF
    Yang, L
    Zhou, H
    Zhong, DF
    PHARMACOGENETICS, 2004, 14 (07): : 465 - 469
  • [32] Identification of a novel ABOA1.02 allele with variant c.671T>C
    Zhang, Jiwei
    He, Yunlei
    Yu, Lu
    Deng, Gang
    TRANSFUSION, 2023, 63 (01) : E4 - E5
  • [33] Identification of a Novel B(972T) Allele in a Blood Donor Associated with B(A) Phenotype
    Konicek, M.
    Vege, S.
    Bensing, K.
    Piefer, C.
    Westhoff, C.
    Ochoa-Garay, G.
    TRANSFUSION, 2023, 63 : 184A - 184A
  • [34] Identification of a novel c.77T>G mutation on the ABO*B.01 allele associated with a B subtype
    Hao, Xiao
    Diao, Xueqin
    Cui, Congcong
    Lv, Yihua
    Liu, Yueqin
    Bi, Huiwen
    TRANSFUSION, 2024, 64 (05) : E21 - E22
  • [35] Identification of a novel A allele with c.478C>T missense mutation on the ABO*A1.02 background
    Deng, Danfei
    Deng, Gang
    He, Yunlei
    Yu, Yong
    TRANSFUSION, 2022, 62 (09) : E47 - E48
  • [36] Identification of a novel RHAG allele with a c.500A>G variation associated with Rhmod phenotype
    Hong, Xiaozhen
    Huang, Xinyu
    Zhang, Jingjing
    Zhu, Faming
    Ying, Yanling
    TRANSFUSION, 2025, 65 (02) : E7 - E9
  • [37] Identification of a novel missense mutation (563G>a) in the ABO gene associated with a Bel phenotype
    Niwa, Reiko
    Nakayama, Takayuki
    Ishii, Hiroyuki
    Fujita, Emi
    Ishiyama, Kazuki
    Matsuo, Tomohito
    Shimizu, Aya
    Gao, Siqiang
    Hayashi, Megumi
    Katai, Akiko
    Ando, Takanori
    Takahashi, Miyuki
    Takeshita, Kyosuke
    Takami, Akiyoshi
    Kato, Hidefumi
    TRANSFUSION, 2016, 56 (05) : 1242 - 1243
  • [38] One novel single nucleotide polymorphism c.424A>G on A1.02 allele in ABO glycosyltransferases leads to A weak phenotype
    Lei, Hang
    Zhang, Hui
    Wang, Yuqing
    Li, Jiaming
    Wang, Xuefeng
    Lou, Can
    Cai, Xiaohong
    JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION, 2024, 123 (11) : 1182 - 1185
  • [39] Identification of a novel frequent RHCE*ce308T variant allele in Chinese D- individuals, resulting in a C plus c- phenotype
    Stegmann, Tamara C.
    Ji, Yanli
    Bijman, Renate
    Wang, Zhen
    Wen, Jizhi
    Wei, Ling
    Veldhuisen, Barbera
    Haer-Wigman, Lonneke
    Lighthart, Peter
    Loden-van Straaten, Martin
    Luo, Guangping
    van der Schoot, C. Ellen
    TRANSFUSION, 2016, 56 (09) : 2314 - 2321
  • [40] Identification of a novel missense mutation (c.608A > G) in the ABO gene contributing to an A variant
    Wu, Xinming
    Ji, Fangyuan
    Huo, Ni
    Wu, Yunping
    Liu, Xinlu
    Zhang, Linhai
    Liang, Wei
    Wang, Zhicheng
    TRANSFUSION, 2020, 60 (09) : E34 - E35