A novel RHD allele caused by c.767 C>T mutation was identified in a Chinese individual

被引：0
|
作者：
Lyu, Hongjuan [1 ]
Wang, Kun [1 ]
Feng, Zhihui [2 ]
Xu, Tao [3 ,4 ]
机构：
[1] Qingdao Women & Childrens Hosp, Obstet Dept, Qingdao, Peoples R China
[2] Qingdao Blood Ctr, Inst Transfus Med, Qingdao, Peoples R China
[3] Qingdao Women & Childrens Hosp, Urol Dept, Qingdao, Peoples R China
[4] Qingdao Women & Childrens Hosp, Urol Dept, 6 Tongfu Rd, Qingdao 266071, Shandong, Peoples R China
来源：
TRANSFUSION | 2024年 / 64卷 / 05期
关键词：
D O I：
10.1111/trf.17820
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
[No abstract available]
引用
收藏
页码：E18 / E20
页数：3
相关论文
共 50 条
  • [1] A novel RHD allele caused by c.739 G> C mutation was identified in a Chinese individual
    Lyu, Hongjuan
    Jiao, Shuxian
    Ma, Wenhui
    Hu, Bin
    TRANSFUSION, 2021, 61 (01) : E1 - E2
  • [2] A novel A allele with c.689G>T mutation identified in a Chinese individual
    Ma, Wenhui
    Feng, Zhihui
    Hu, Bin
    Han, Bin
    Jiao, Shuxian
    TRANSFUSION, 2018, 58 (09) : 2250 - 2251
  • [3] A novel A allele with the 595C>T mutation identified in a Chinese individual with the Am phenotype
    Tian, L.
    Yao, Z. -Q.
    Deng, Y. -F.
    Hong, L.
    Song, N.
    TRANSFUSION MEDICINE, 2013, 23 (02) : 134 - 135
  • [4] A novel B allele with c.502C>G mutation identified in a Chinese individual
    Chen, Qing
    Xiao, Jianyu
    Lu, Le
    Du, Leilei
    Huang, Chengyin
    Li, Min
    Li, Ping
    Yao, Genhong
    TRANSFUSION, 2015, 55 (06) : 1582 - 1583
  • [5] A new RHD variant allele caused by an RHD c.1228-1G>C mutation in a Chinese family
    Wu, Fan
    Liang, Shuang
    Zhuang, Nai-Bao
    Su, Yu-Qing
    Liang, Yan-Lian
    Peng, Long
    Xu, Yun-Ping
    Shao, Chao-Peng
    TRANSFUSION, 2021, 61 (09) : E55 - E56
  • [6] A novel A allele with c.287G > T mutation identified in a Chinese family
    Ma, Wenhui
    Zhang, Shuchao
    Jiao, Shuxian
    Feng, Zhihui
    TRANSFUSION, 2020, 60 (07) : E19 - E20
  • [7] A new RHD variant allele is caused by a RHD 662C>G mutation
    Feng, Jing
    Tian, Li
    Chen, Jian
    TRANSFUSION, 2017, 57 (06) : 1566 - 1567
  • [8] A novel missense mutation (c.221G>C) in RHD gene identified in a Chinese woman
    Lai, Shichao
    Tian, Li
    Hou, Li
    TRANSFUSION, 2022, 62 (07) : E30 - E31
  • [9] A novel A allele with c.499G>A mutation identified in a Chinese individual
    Han, Bin
    Liu, Li
    Feng, Zhihui
    Bu, Xiangmao
    TRANSFUSION, 2020, 60 (06) : E15 - E16
  • [10] A novel A allele with c.963_964insC mutation identified in a Chinese individual
    Liu, Li
    Chi, Xiaoyun
    Bu, Xiangmao
    Feng, Zhihui
    Su, Nailun
    TRANSFUSION, 2021, 61 (01) : E7 - E8
12345