Detection of Mutations in LRPAP1, CTSH, LEPREL1, ZNF644, SLC39A5, and SCO2 in 298 Families With Early-Onset High Myopia by Exome Sequencing-Reference-Cited by-同舟云学术

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Detection of Mutations in LRPAP1, CTSH, LEPREL1, ZNF644, SLC39A5, and SCO2 in 298 Families With Early-Onset High Myopia by Exome Sequencing

Published:2014-12-18 Issue:1 Volume:56 Page:339-345
ISSN:0146-0404
Container-title:Investigative Ophthalmology & Visual Science
language:en
Short-container-title:Investigative Ophthalmology & Visual Science

Author:

Jiang D.,Li J.,Xiao X.,Li S.,Jia X.,Sun W.,Guo X.,Zhang Q.

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

Cited by 92 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. Link between parental myopia and early‐onset high myopia: Insights from a clinical retrospective analysis;Ophthalmic and Physiological Optics;2024-05-27

2. Clinical features of patients with mutations in genes for nanophthalmos;British Journal of Ophthalmology;2024-05-14

3. Trio-based whole-exome sequencing reveals mutations in early-onset high myopia;BMJ Open Ophthalmology;2024-05

4. Double Hyperautofluorescence Rings as a Sign of CFAP410-related Retinopathy;Investigative Opthalmology & Visual Science;2023-12-28

5. Exome sequencing on 20 probands with early-onset high myopia: identify variants in Retnet genes and interacting of genes in the candidate genes;2023-12-08

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