A novel RNA-splicing mutation in TRAPPC2 gene causing X-linked spondyloepiphyseal dysplasia tarda in a large Chinese family

被引:0
|
作者
Hong Guo
Xueqing Xu
Kai Wang
Bo Zhang
Guohong Deng
Yan Wang
Yun Bai
机构
[1] Third Military Medical University,Department of Medical Genetics
[2] Third Military Medical University,Department of Infectious Diseases, Southwest Hospital
来源
Journal of Genetics | 2009年 / 88卷
关键词
X-linked spondyloepiphyseal dysplasia tarda (SEDT); trafficking protein particle complex 2 (; ); mutation; alternate splicing; human genetics; Chinese population;
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
页码:87 / 91
页数:4
相关论文
共 50 条
  • [31] A novel missense mutation in collagenous domain of EDA gene in a Chinese family with X-linked hypohidrotic ectodermal dysplasia
    Li, Daxu
    Xu, Ran
    Huang, Fumeng
    Wang, Biyuan
    Tao, Yu
    Jiang, Zijian
    Li, Hairui
    Yao, Jianfeng
    Xu, Peng
    Wu, Xiaokang
    Ren, Le
    Zhang, Rui
    Kelsoe, John R.
    Ma, Jie
    JOURNAL OF GENETICS, 2015, 94 (01) : 115 - 119
  • [32] AN RNA-SPLICING MUTATION (G(+51VS20)) IN THE TYPE-II COLLAGEN GENE (COL2AI) IN A FAMILY WITH SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA
    TILLER, GE
    WEIS, MA
    POLUMBO, PA
    GRUBER, HE
    RIMOIN, DL
    COHN, DH
    EYRE, DR
    AMERICAN JOURNAL OF HUMAN GENETICS, 1995, 56 (02) : 388 - 395
  • [33] The family reported to have X-linked Dyggve-Melchior-Clausen syndrome instead has X-linked SEDT caused by a novel TRAPPC2 frameshift variant
    Yunis, Juan J. J.
    Yunis, Luz K. K.
    CLINICAL GENETICS, 2023, 103 (06) : 720 - 722
  • [34] A novel EDA gene mutation in a Spanish family with X-linked hypohidrotic ectodermal dysplasia
    Canueto, J.
    Zafra-Cobo, M. I.
    Ciria, S.
    Unamuno, P.
    Gonzalez-Sarmiento, R.
    ACTAS DERMO-SIFILIOGRAFICAS, 2011, 102 (09): : 722 - 725
  • [35] A novel mutation of RPGR gene in an X-Linked Chinese family with retinitis pigmentosa
    Li, Ningdong
    Dai, Shuzhen
    Zhang, Liling
    Mei, Han
    Wang, Liming
    MOLECULAR GENETICS AND METABOLISM, 2011, 102 (04) : 488 - 493
  • [36] A novel GPR143 splicing mutation in a Chinese family with X-linked congenital nystagmus
    Hu, Junjie
    Liang, Desheng
    Xue, Jinjie
    Liu, Jing
    Wu, Lingqian
    MOLECULAR VISION, 2011, 17 (81-82): : 715 - 722
  • [37] A novel gene mutation in a family with X-linked retinoschisis
    Lai, Yu-Hung
    Huang, Shun-Ping
    Chen, Shee-Ping
    Hu, Pei-Shin
    Lin, Shu-Fung
    Sheu, Min-Muh
    Wang, Hwei-Zu
    Tsai, Rong Kung
    JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION, 2015, 114 (09) : 872 - 880
  • [38] Identification of a Novel Mutation in the COL2A1 Gene in a Chinese Family with Spondyloepiphyseal Dysplasia Congenita
    Huang, Xiangjun
    Deng, Xiong
    Xu, Hongbo
    Wu, Song
    Yuan, Lamei
    Yang, Zhijian
    Yang, Yan
    Deng, Hao
    PLOS ONE, 2015, 10 (06):
  • [39] A novel frameshift mutation of the EDA1 gene in a Chinese Han family with X-linked hypohidrotic ectodermal dysplasia
    Zhang, H.
    Quan, C.
    Sun, L. -D.
    Lv, H. -L.
    Gao, M.
    Zhou, F. -S.
    Xiao, F. -L.
    Fang, Q. -Y.
    Shen, Y. -J.
    Zhou, L.
    Yang, S.
    Zhang, X. -J.
    CLINICAL AND EXPERIMENTAL DERMATOLOGY, 2009, 34 (01) : 74 - 76
  • [40] Co-occurrence of Spondyloepiphyseal Dysplasia and X-Linked Hypophosphatemia in a Three-Generation Chinese Family
    Jian Ma
    Ye Zhang
    Xiaoxiao Ding
    Zhijiang Liang
    Chaoxiang Yang
    Zhi Deng
    Hui He
    Zhihong Guan
    Chunhua Zeng
    Yunting Lin
    Xianqiong Luo
    Calcified Tissue International, 2023, 113 : 266 - 275