Literature DB >> 26425852

Correction: Novel Compound Heterozygous Mutations in MYO7A Associated with Usher Syndrome 1 in a Chinese Family.

Xue Gao, Guo-Jian Wang, Yong-Yi Yuan, Feng Xin, Ming-Yu Han, Jing-Qiao Lu, Hui Zhao, Fei Yu, Jin-Cao Xu, Mei-Guang Zhang, Jiang Dong, Xi Lin, Pu Dai.   

Abstract

Entities:  

Year:  2015        PMID: 26425852      PMCID: PMC4591013          DOI: 10.1371/journal.pone.0137883

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.240


× No keyword cloud information.
The following information is missing from the Competing Interests section: “Xi Lin owns stocks in Otogenetics Corporation, which may be a source of potential conflict of interest for materials presented in this paper. This does not alter our adherence to PLOS ONE policies on sharing data and materials.”
  1 in total

1.  Novel compound heterozygous mutations in MYO7A Associated with Usher syndrome 1 in a Chinese family.

Authors:  Xue Gao; Guo-Jian Wang; Yong-Yi Yuan; Feng Xin; Ming-Yu Han; Jing-Qiao Lu; Hui Zhao; Fei Yu; Jin-Cao Xu; Mei-Guang Zhang; Jiang Dong; Xi Lin; Pu Dai
Journal:  PLoS One       Date:  2014-07-31       Impact factor: 3.240

  1 in total
  1 in total

1.  Comprehensive genetic testing of Chinese SNHL patients and variants interpretation using ACMG guidelines and ethnically matched normal controls.

Authors:  Yongyi Yuan; Qi Li; Yu Su; Qiongfen Lin; Xue Gao; Hankui Liu; Shasha Huang; Dongyang Kang; N Wendell Todd; Douglas Mattox; Jianguo Zhang; Xi Lin; Pu Dai
Journal:  Eur J Hum Genet       Date:  2019-09-20       Impact factor: 4.246

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.