A Novel Mutation in CRYGC Mutation Associated with Autosomal Dominant Congenital Cataracts and Microcornea-Reference-Cited by-同舟云学术

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A Novel Mutation in CRYGC Mutation Associated with Autosomal Dominant Congenital Cataracts and Microcornea

Published:2022-03 Issue:1 Volume:2 Page:100093
ISSN:2666-9145
Container-title:Ophthalmology Science
language:en
Short-container-title:Ophthalmology Science

Author:

Zhou Zhenbao,Zhao Liying,Guo Yanqin,Zhuang Jingyi,Zhuo Nan,Chen Han,Liu Jieting,Wang Libo

Funder

Natural Science Foundation of Heilongjiang Province

Publisher

Elsevier BV

Subject

General Materials Science

Reference49 articles.

1. A novel mutation in the CRYAA gene associated with congenital cataract and microphthalmia in a Chinese family;Song;BMC Med Genet,2018

2. The genetics of cataract: our vision becomes clearer;Hejtmancik;Am J Hum Genet,1998

3. X-linked inheritances recessive of congenital nystagmus and autosomal dominant inheritances of congenital cataracts coexist in a Chinese family: a case report and literature review;Yan;BMC Med Genet,2019

4. Genetics of human cataract;Shiels;Clin Genet,2013

5. A novel mutation in the OAR domain of PITX3 associated with congenital posterior subcapsular cataract;Fan;BMC Med Genet,2019

Cited by 2 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. Novel compound heterozygous variants in LTBP2 associated with relative anterior microphthalmos;European Journal of Ophthalmology;2024-03-28

2. Novel CRYGC Mutation in Conserved Ultraviolet-Protective Tryptophan (p.Trp131Arg) Is Linked to Autosomal Dominant Congenital Cataract;International Journal of Molecular Sciences;2023-11-22

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