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Clinical science
Fibrillin-1 gene mutations in a Chinese cohort with congenital ectopia lentis: spectrum and genotype–phenotype analysis

Authors

  • Zexu Chen Eye Institute and Department of Ophthalmology, Eye & ENT Hospital, Fudan University, Shanghai, China NHC Key Laboratory of Myopia (Fudan University), Key Laboratory of Myopia, Chinese Academy of Medical Sciences, Shanghai, China Shanghai Key Laboratory of Visual Impairment and Restoration, Shanghai, China PubMed articlesGoogle scholar articles
  • Tianhui Chen Eye Institute and Department of Ophthalmology, Eye & ENT Hospital, Fudan University, Shanghai, China NHC Key Laboratory of Myopia (Fudan University), Key Laboratory of Myopia, Chinese Academy of Medical Sciences, Shanghai, China Shanghai Key Laboratory of Visual Impairment and Restoration, Shanghai, China PubMed articlesGoogle scholar articles
  • Min Zhang Eye Institute and Department of Ophthalmology, Eye & ENT Hospital, Fudan University, Shanghai, China NHC Key Laboratory of Myopia (Fudan University), Key Laboratory of Myopia, Chinese Academy of Medical Sciences, Shanghai, China Shanghai Key Laboratory of Visual Impairment and Restoration, Shanghai, China PubMed articlesGoogle scholar articles
  • Jiahui Chen Eye Institute and Department of Ophthalmology, Eye & ENT Hospital, Fudan University, Shanghai, China NHC Key Laboratory of Myopia (Fudan University), Key Laboratory of Myopia, Chinese Academy of Medical Sciences, Shanghai, China Shanghai Key Laboratory of Visual Impairment and Restoration, Shanghai, China PubMed articlesGoogle scholar articles
  • Michael Deng Eye Institute and Department of Ophthalmology, Eye & ENT Hospital, Fudan University, Shanghai, China NHC Key Laboratory of Myopia (Fudan University), Key Laboratory of Myopia, Chinese Academy of Medical Sciences, Shanghai, China Shanghai Key Laboratory of Visual Impairment and Restoration, Shanghai, China PubMed articlesGoogle scholar articles
  • Jialei Zheng Eye Institute and Department of Ophthalmology, Eye & ENT Hospital, Fudan University, Shanghai, China NHC Key Laboratory of Myopia (Fudan University), Key Laboratory of Myopia, Chinese Academy of Medical Sciences, Shanghai, China Shanghai Key Laboratory of Visual Impairment and Restoration, Shanghai, China PubMed articlesGoogle scholar articles
  • Li-Na Lan Eye Institute and Department of Ophthalmology, Eye & ENT Hospital, Fudan University, Shanghai, China NHC Key Laboratory of Myopia (Fudan University), Key Laboratory of Myopia, Chinese Academy of Medical Sciences, Shanghai, China Shanghai Key Laboratory of Visual Impairment and Restoration, Shanghai, China PubMed articlesGoogle scholar articles
  • Yongxiang Jiang Eye Institute and Department of Ophthalmology, Eye & ENT Hospital, Fudan University, Shanghai, China NHC Key Laboratory of Myopia (Fudan University), Key Laboratory of Myopia, Chinese Academy of Medical Sciences, Shanghai, China Shanghai Key Laboratory of Visual Impairment and Restoration, Shanghai, China PubMed articlesGoogle scholar articles
  1. Correspondence to Professor Yongxiang Jiang, Fudan University Eye Ear Nose and Throat Hospital Department of Ophthalmology, Shanghai, China; yongxiang_jiang{at}163.com
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Citation

Chen Z, Chen T, Zhang M, et al
Fibrillin-1 gene mutations in a Chinese cohort with congenital ectopia lentis: spectrum and genotype–phenotype analysis
British Journal of Ophthalmology 2022;106:1655-1661.

Publication history

  • Received March 8, 2021
  • Accepted July 2, 2021
  • First published July 19, 2021.
Online issue publication 
March 06, 2023

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© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.