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Current Eye Research Volume 35, 2010 - Issue 6
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Original Article

Autosomal Dominant Congenital Nuclear Cataracts Caused by a CRYAA Gene Mutation

Fei-Feng Li
,
Min YangBeijing Tongren Eye Center, Capital Medical University, Beijing, China
,
Xu Ma
,
Qiong ZhangDepartment of Antibiotics, Qiqihar Drug Testing Institute, Heilongjiang, Qiqihar, China
,
Meng ZhangGraduate School, Peking Union Medical College, Beijing, China
,
Shu-Zhen WangBeijing Tongren Eye Center, Capital Medical University, Beijing, China
&
Si-Quan ZhuBeijing Tongren Eye Center, Capital Medical University, Beijing, ChinaCorrespondence[email protected]
 show all
Pages 492-498 | Received 22 Mar 2009, Accepted 06 Jan 2010, Published online: 14 May 2010

Citations (10)

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Read on this site (3)

Zhennan Zhao, Jiahui Chen, Wenyi Yuan, Yongxiang Jiang & Yi Lu. (2023) Association between single nucleotide polymorphisms in exon 3 of the alpha-A-crystallin gene and susceptibility to age-related cataract. Ophthalmic Genetics 44:2, pages 127-132.
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Kai Jie Wang, Xu Zha, Dou Dou Chen & Si Quan Zhu. (2018) Mutation Analysis of Families with Autosomal Dominant Congenital Cataract: A Recurrent Mutation in the CRYBA1/A3 Gene Causing Congenital Nuclear Cataract. Current Eye Research 43:3, pages 304-307.
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Joanne E Sutherland & Megan A Day. (2011) Advantages and disadvantages of molecular testing in ophthalmology. Expert Review of Ophthalmology 6:2, pages 221-245.
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Articles from other publishers (7)

Prashanth Budnar, Ramakrishna Tangirala, Raman Bakthisaran & Ch. Mohan Rao. (2022) Protein Aggregation and Cataract: Role of Age-Related Modifications and Mutations in α-Crystallins. Biochemistry (Moscow) 87:3, pages 225-241.
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B. Tedesco, R. Cristofani, V. Ferrari, M. Cozzi, P. Rusmini, E. Casarotto, M. Chierichetti, F. Mina, M. Galbiati, M. Piccolella, V. Crippa & A. Poletti. (2022) Insights on Human Small Heat Shock Proteins and Their Alterations in Diseases. Frontiers in Molecular Biosciences 9.
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Hongli Zhu & Zhichang Zhang. (2021) Emerging Trends and Research Foci in Cataract Genes: A Bibliometric and Visualized Study. Frontiers in Genetics 12.
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Shari Javadiyan, Jamie E. Craig, Emmanuelle Souzeau, Shiwani Sharma, Karen M. Lower, John Pater, Theresa Casey, Trevor Hodson & Kathryn P. Burdon. (2016) Recurrent mutation in the crystallin alpha A gene associated with inherited paediatric cataract. BMC Research Notes 9:1.
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Alok Kumar Panda, Sandip Kumar Nandi, Ayon Chakraborty, Ram H. Nagaraj & Ashis Biswas. (2016) Differential role of arginine mutations on the structure and functions of α-crystallin. Biochimica et Biophysica Acta (BBA) - General Subjects 1860:1, pages 199-210.
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Xueyuan Jia, Feng Zhang, Jing Bai, Linghan Gao, Xuelong Zhang, Haiming Sun, Donglin Sun, Rongwei Guan, Wenjing Sun, Lidan Xu, Zhichao Yue, Yang Yu & Songbin Fu. (2013) Combinational analysis of linkage and exome sequencing identifies the causative mutation in a Chinese family with congenital cataract. BMC Medical Genetics 14:1.
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Konstantinos Sousounis & Panagiotis A Tsonis. (2012) Patterns of gene expression in microarrays and expressed sequence tags from normal and cataractous lenses. Human Genomics 6:1.
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