A novel cis-AB allele derived from a unique 796 C>A mutation in exon 7 ABO gene (vol 45, pg 50, 2005)

被引:0
|
作者
Tzeng, CH
Chen, YJ
Lyou, JY
Chen, PS
Liu, HM
Hu, HY
Lin, JS
Yu, LC
机构
关键词
D O I
10.1111/j.1537-2995.2005.00623.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:1827 / 1827
页数:1
相关论文
共 10 条
  • [1] A novel cis-AB allele derived from a unique 796C>A mutation in exon 7 of ABO gene
    Tzeng, CH
    Chen, YJ
    Lyou, JY
    Chen, PS
    Liu, HM
    Hu, HY
    Lin, JS
    Yu, LC
    TRANSFUSION, 2005, 45 (01) : 50 - 55
  • [2] A novel cis-AB allele derived from the A transferase gene by nucleotide substitution C796A
    Chen, DP
    Tseng, CP
    Wang, WT
    Wang, MC
    Tsao, KC
    Wu, TL
    Sun, CF
    ANNALS OF CLINICAL AND LABORATORY SCIENCE, 2004, 34 (04): : 437 - 442
  • [3] A novel cis-AB variant allele arising from a nucleotide substitution A796C in the B transferase gene
    Mifsud, NA
    Watt, JM
    Condon, JA
    Haddad, AP
    Sparrow, RL
    TRANSFUSION, 2000, 40 (10) : 1276 - 1277
  • [4] A novel cis-AB allele with c.797T>C mutation identified in three unrelated Chinese individuals
    Zhang, Xu
    Li, Jianping
    TRANSFUSION, 2018, 58 (10) : 2463 - 2464
  • [5] A cis-AB Variant Allele Arising from a de novo Nucleotide Substitution A796C in the B Glycosyltransferase Gene
    He, B.
    TRANSFUSION, 2016, 56 : 154A - 155A
  • [6] A novel cis-AB variant allele arising from a de novo nucleotide substitution c.796A>G (p.M266V) in the B glycosyltransferase gene
    Lee, S. Y.
    Phan, M. T. T.
    Shin, D. J.
    Shin, M. G.
    Park, J. T.
    Shin, J. W.
    Yazer, M. H.
    Shin, H. B.
    Cho, D.
    TRANSFUSION MEDICINE, 2015, 25 (05) : 333 - 336
  • [7] A unique 502C>T mutation in exon 7 of ABO gene associated with the Bel phenotype in Taiwan
    Lin, PH
    Li, L
    Lin-Tsai, SJ
    Lin, KT
    Chen, JM
    Chu, DC
    TRANSFUSION, 2003, 43 (09) : 1254 - 1259
  • [8] A novel all Ael derived from a unique 816insG in Exon 7 of the ABO gene
    Liu, Hsueng-Mei
    Chen, Ying-Ju
    Chen, Pei-Shan
    Lyou, Jau-Yi
    Hu, Hui-Yu
    Ho, Yung-Tai
    Lin, Jeong-Shi
    Tzeng, Cheng-Hwai
    JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION, 2007, 106 (11) : 969 - 974
  • [9] Novel mutation c.980_983delATTA compound with c.986C>A mutation of the FRMD7 gene in a Chinese family with X-linked idiopathic congenital nystagmus (vol 14, pg 479, 2013)
    Song, Feng-wei
    Chen, Bin-bin
    Sun, Zhao-hui
    Wu, Li-ping
    Zhao, Su-juan
    Miao, Qi
    Tang, Xia-jing
    JOURNAL OF ZHEJIANG UNIVERSITY-SCIENCE B, 2013, 14 (09): : 866 - 866
  • [10] A novel point mutation (R243Q) in exon 7 of the c-erbA beta thyroid hormone receptor gene in a family with resistance to thyroid hormone (vol 5, pg 355, 1995)
    Onigata, K
    Yagi, H
    Sakurai, A
    Nagashima, T
    Nomura, Y
    Nagashima, K
    Hashizume, K
    Morikawa, A
    THYROID, 1995, 5 (06) : 508 - 508