CCDC66mutations are associated with high myopia through affected cell mitosis
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Title
CCDC66mutations are associated with high myopia through affected cell mitosis
Authors
Keywords
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Journal
JOURNAL OF MEDICAL GENETICS
Volume -, Issue -, Pages jmg-2023-109434
Publisher
BMJ
Online
2023-10-19
DOI
10.1136/jmg-2023-109434
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- (2020) Paul N. Baird et al. Nature Reviews Disease Primers
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- (2019) Xue-Bi Cai et al. EXPERIMENTAL EYE RESEARCH
- Centrosomal and ciliary targeting of CCDC66 requires cooperative action of centriolar satellites, microtubules and molecular motors
- (2019) Deniz Conkar et al. Scientific Reports
- Myopia: is the nature‐nurture debate finally over?
- (2018) Ian G Morgan et al. Clinical and Experimental Optometry
- The centriolar satellite protein CCDC66 interacts with CEP290 and functions in cilium formation and trafficking
- (2017) Deniz Conkar et al. JOURNAL OF CELL SCIENCE
- Global Prevalence of Myopia and High Myopia and Temporal Trends from 2000 through 2050
- (2016) Brien A. Holden et al. OPHTHALMOLOGY
- Mechanism of microtubule lumen entry for the α-tubulin acetyltransferase enzyme αTAT1
- (2016) Courtney Coombes et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
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- (2015) Lin Li et al. CELLULAR AND MOLECULAR LIFE SCIENCES
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- (2015) Hui Guo et al. GENETICS IN MEDICINE
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- (2014) Hui Guo et al. JOURNAL OF MEDICAL GENETICS
- Mutations in LRPAP1 Are Associated with Severe Myopia in Humans
- (2013) Mohammed A. Aldahmesh et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Genome-Wide Analysis Points to Roles for Extracellular Matrix Remodeling, the Visual Cycle, and Neuronal Development in Myopia
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- (2012) Erin A. Bassett et al. TRENDS IN NEUROSCIENCES
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- (2011) Wanda M. Gerding et al. HUMAN MOLECULAR GENETICS
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- (2010) Heng Li et al. BIOINFORMATICS
- ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
- (2010) K. Wang et al. NUCLEIC ACIDS RESEARCH
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