Erratum to: Identification of a novel mutation in a Chinese family with Nance-Horan syndrome by whole exome sequencing

被引:0
|
作者
Nan HONG [1 ]
Yan-hua CHEN [2 ]
Chen XIE [1 ]
Bai-sheng XU [1 ]
Hui HUANG [2 ]
Xin LI [2 ]
Yue-qing YANG [2 ]
Ying-ping HUANG [2 ]
Jian-lian DENG [2 ]
Ming QI [2 ,3 ,4 ]
Yang-shun GU [1 ]
机构
[1] Department of Ophthalmology,the First Affiliated Hospital,School of Medicine,Zhejiang University
[2] Beijing Genomics Institute (BGI)-Shenzhen
[3] School of Basic Medical Sciences,Zhejiang University
[4] Functional Genomics Center,Department of Pathology&Laboratory Medicine,University of Rochester Medical Center
关键词
Erratum to; Identification of a novel mutation in a Chinese family with Nance-Horan syndrome by whole exome sequencing;
D O I
暂无
中图分类号
+ [];
学科分类号
摘要
Erratum to:J Zhejiang Univ-Sci B(Biomed&Biotechnol)2014 15(8):727-734doi:10.1631/jzus.B1300321The original version of this article unfortunately contained a mistake.In the authors"Nan HONG§1,Yan-hua CHEN§1,Chen XIE1,Bai-sheng XU1,Hui HUANG2,Xin LI2,Yue-qing YANG2,Ying-ping HUANG2,Jian-lian DENG2,Ming QI2,3,4,Yangshun GU1",the superscript sequence number"1",
引用
收藏
页码:1011 / 1011
页数:1
相关论文
共 50 条
  • [41] Genotype-Phenotype Correlations of Nance-Horan Syndrome in Male and Female Carriers of a Novel Variant
    Zin, Olivia A.
    Neves, Luiza M.
    Motta, Fabiana L.
    Junior, Daltro C.
    Cunha, Daniela P.
    Agonigi, Bruna N. S.
    Malacarne, Jocieli
    Rodrigues, Ana Paula S.
    Rodrigues, Gabriela D.
    Tinoco, Maria Luisa C.
    Horovitz, Dafne D. G.
    Carvalho, Adriana B.
    Zin, Andrea A.
    Vasconcelos, Zilton F. M.
    Sallum, Juliana M. Ferraz
    GENES, 2025, 16 (01)
  • [42] Identification of Causative Mutation in a Korean Family with Crouzon Syndrome Using Whole Exome Sequencing
    Sagong, Borum
    Jung, Da Jung
    Baek, Jeong-In
    Kim, Min-A
    Lee, Jaetae
    Lee, Sang-Heun
    Kim, Un-Kyung
    Lee, Kyu-Yup
    ANNALS OF CLINICAL AND LABORATORY SCIENCE, 2014, 44 (04): : 476 - 483
  • [43] Identification of a mutL-homolog 1 mutation via whole-exome sequencing in a Chinese family with Gardner syndrome
    Lv, Zilan
    Wang, Chuan
    Wu, Lixiang
    Guo, Bianqin
    Zhang, Darong
    Hang, Yang
    Huang, Shengxing
    Ou, Minglin
    MOLECULAR MEDICINE REPORTS, 2018, 18 (01) : 987 - 992
  • [44] Whole-exome sequencing identification of a novel splicing mutation of RUNX2 in a Chinese family with cleidocranial dysplasia
    Zhang, Tingting
    Wu, Jing
    Zhao, Xiaoxue
    Hou, Feifei
    Ma, Tengfei
    Wang, Huijuan
    Zhang, Xu
    Zhang, Xiangyu
    ARCHIVES OF ORAL BIOLOGY, 2019, 100 : 49 - 56
  • [45] Identification of a novel mutation site in maturity-onset diabetes of the young in a Chinese family by whole-exome sequencing
    Yu, Han
    Liu, Jingjin
    Li, Xiaofei
    Miao, Fang
    Yang, Yanlan
    MOLECULAR MEDICINE REPORTS, 2019, 20 (03) : 2373 - 2380
  • [46] Identification of a Novel VPS13B Mutation in a Chinese Patient with Cohen Syndrome by Whole-Exome Sequencing
    Hu, Xiaoyun
    Huang, Tao
    Liu, Yun
    Zhang, Lina
    Zhu, Li
    Peng, Xiaohong
    Zhang, Sufang
    PHARMACOGENOMICS & PERSONALIZED MEDICINE, 2021, 14 : 1583 - 1589
  • [47] Identification of a novel mutation in ALMS1 in a Chinese patient with monogenic diabetic syndrome by whole-exome sequencing
    Zhong, Ming
    Huang, Ling-Ning
    Zhang, Song-Jing
    Yan, Sun-Jie
    NIGERIAN JOURNAL OF CLINICAL PRACTICE, 2022, 25 (12) : 2077 - 2080
  • [48] Identification of a Novel Twinkle Mutation in a Family With Infantile Onset Spinocerebellar Ataxia by Whole Exome Sequencing
    Dundar, Hall
    Ozgul, Riza Koksal
    Yalnizoglu, Dilek
    Erdem, Sevim
    Oguz, Kader Karli
    Tuncel, Deniz
    Temucin, Cagri Mesut
    Dursun, Ali
    PEDIATRIC NEUROLOGY, 2012, 46 (03) : 172 - 177
  • [49] Novel causative mutations in patients with Nance-Horan syndrome and altered localization of the mutant NHS-A protein isoform
    Sharma, Shiwani
    Burdon, Kathryn P.
    Dave, Alpana
    Jamieson, Robyn V.
    Yaron, Yuval
    Billson, Frank
    Van Maldergem, Lionel
    Lorenz, Birgit
    Gecz, Jozef
    Craig, Jamie E.
    MOLECULAR VISION, 2008, 14 (219-23): : 1856 - 1864
  • [50] Identification of a novel MIP frameshift mutation associated with congenital cataract in a Chinese family by whole-exome sequencing and functional analysis
    Xigui Long
    Yanru Huang
    Hu Tan
    Zhuo Li
    Rui Zhang
    Siyuan Linpeng
    Weigang Lv
    Yingxi Cao
    Haoxian Li
    Desheng Liang
    Lingqian Wu
    Eye, 2018, 32 : 1359 - 1364