CCDC111 mutation was identified in high myopia through exome sequencing

被引：0
|
作者：
Zhao, Fuxin [1 ]
Zhou, Xiangtian [1 ]
Xue, Anquan [1 ]
Su, Yanfeng [1 ]
Qu, Jia [1 ]
机构：
[1] Wenzhou Med Coll, Sch Ophthal & Optometry, Wenzhou, Peoples R China
来源：
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | 2013年 / 54卷 / 15期
关键词：
539; genetics; 605; myopia;
D O I：
暂无
中图分类号：
R77 [眼科学];
学科分类号：
100212 ;
摘要：
3361
引用
收藏
页数：2
相关论文
共 50 条
  • [1] Exome sequencing reveals CCDC111 mutation associated with high myopia
    Fuxin Zhao
    Jinyu Wu
    Anquan Xue
    Yanfeng Su
    Xiaojing Wang
    Xianmin Lu
    Zhonglou Zhou
    Jia Qu
    Xiangtian Zhou
    Human Genetics, 2013, 132 : 913 - 921
  • [2] Exome sequencing reveals CCDC111 mutation associated with high myopia
    Zhao, Fuxin
    Wu, Jinyu
    Xue, Anquan
    Su, Yanfeng
    Wang, Xiaojing
    Lu, Xianmin
    Zhou, Zhonglou
    Qu, Jia
    Zhou, Xiangtian
    HUMAN GENETICS, 2013, 132 (08) : 913 - 921
  • [3] The diagnostic yield of whole exome sequencing in high myopia
    Haarman, Annechien E. G.
    Thiadens, Alberta A. H. J.
    Polling, Jan Roelof
    De Klein, Annelies J. E. M. M.
    Brosens, Erwin
    Van Tienhoven, Marianne
    Loudon, Sjoukje E.
    Bouman, Arjan
    Kievit, Anneke J. A.
    Hoefsloot, Lies H.
    Klaver, Caroline C. W.
    Verhoeven, Virginie J. M.
    ACTA OPHTHALMOLOGICA, 2021, 99 : 38 - 38
  • [4] Exome sequencing study of 20 patients with high myopia
    Wan, Ling
    Deng, Boling
    Wu, Zhengzheng
    Chen, Xiaoming
    PEERJ, 2018, 6
  • [5] Diagnostic exome sequencing in 50 patients with high myopia
    Verhoeven, Virginie
    Haarman, Annechien
    Polling, Jan Roelof
    van Tienhoven, Marianne
    Thiadens, Alberta
    Loudon, Sjoukje E.
    Bouman, Arjan
    Kievit, Anneke J. A.
    Hoefsloot, Lies H.
    Klaver, Caroline
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2020, 61 (07)
  • [6] Diagnostic exome sequencing in 50 patients with high myopia
    Verhoeven, V. J. M.
    Haarman, A. E. G.
    van Tienhoven, M.
    Thiadens, A. A. H. J.
    Loudon, S. E.
    de Klein, A.
    Brosens, E.
    Polling, J. R.
    Bouman, A.
    Klaver, C. C. W.
    Kievit, A. J. A.
    Hoefsloot, L. H.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2020, 28 (SUPPL 1) : 195 - 195
  • [7] Exome sequencing identified null mutations in LOXL3 associated with early-onset high myopia
    Li, Jiali
    Gao, Bei
    Xiao, Xueshan
    Li, Shiqiang
    Jia, Xiaoyun
    Sun, Wenmin
    Guo, Xiangming
    Zhang, Qingjiong
    MOLECULAR VISION, 2016, 22 : 161 - 167
  • [8] New heritable ATRX mutation identified by whole exome sequencing and review
    Shahbazi, Zahra
    Rostami, Golaleh
    Hamid, Mohammad
    EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS, 2022, 23 (01)
  • [9] New heritable ATRX mutation identified by whole exome sequencing and review
    Zahra Shahbazi
    Golaleh Rostami
    Mohammad Hamid
    Egyptian Journal of Medical Human Genetics, 23
  • [10] Exome Sequencing of Pancreatic Acinar Carcinoma Identified Distinctive Mutation Patterns
    Liu, Yuanhang
    Raimondo, Massimo
    Wallace, Michael B.
    Mody, Kabir
    Stauffer, John A.
    Zhang, Lizhi
    Ji, Baoan
    Bi, Yan
    PANCREAS, 2021, 50 (07) : 1007 - 1013
12345