Mutation Analysis of Families with Autosomal Dominant Congenital Cataract: A Recurrent Mutation in the CRYBA1/A3 Gene Causing Congenital Nuclear Cataract-Reference-Cited by-同舟云学术

Mutation Analysis of Families with Autosomal Dominant Congenital Cataract: A Recurrent Mutation in the CRYBA1/A3 Gene Causing Congenital Nuclear Cataract

Published:2018-01-24 Issue:3 Volume:43 Page:304-307
ISSN:0271-3683
Container-title:Current Eye Research
language:en
Short-container-title:Current Eye Research

Author:

Wang Kai Jie¹,Zha Xu²,Chen Dou Dou¹,Zhu Si Quan¹

Affiliation:

1. Beijing Tongren Eye Center, Beijing Tongren Hospital, Capital Medical University,Beijing Ophthalmology & Visual Sciences Key Lab, Beijing, China

2. Department of Ophthalmology, the Second Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China

Funder

Beijing Nova Program

National Natural Science Foundation of China

Natural Science Foundation of Beijing Municipality

the priming scientific research foundation for the senior researchers in Beijing Tongren Hospital, Capital Medical University

Publisher

Informa UK Limited

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

Link

https://www.tandfonline.com/doi/pdf/10.1080/02713683.2017.1406527

Reference22 articles.

1. Molecular genetic basis of inherited cataract and associated phenotypes

2. Autosomal Dominant Congenital Nuclear Cataracts Caused by a CRYAA Gene Mutation

3. Next-generation sequencing for D47N mutation in Cx50 analysis associated with autosomal dominant congenital cataract in a six-generation Chinese family

4. Congenital cataracts and their molecular genetics

5. Novel β-Crystallin Gene Mutations in Chinese Families With Nuclear Cataracts

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Lens;Ocular Pathology;2025

2. Dysregulation of Autophagy Occurs During Congenital Cataract Development in βA3ΔG91 Mice;Investigative Opthalmology & Visual Science;2024-04-01

3. Identification of pathogenic genetic variants in patients with acquired early-onset bilateral cataracts using next-generation sequencing;Journal of American Association for Pediatric Ophthalmology and Strabismus;2024-02

4. Congenital Cataract and Its Genetics: The Era of Next-Generation Sequencing;Turkish Journal of Ophthalmology;2021-04-29

5. A novel missense mutation of CRYBA1 in a northern Chinese family with inherited coronary cataract with blue punctate opacities;European Journal of Ophthalmology;2021-04-07