Homozygous loss-of-function mutation of theLEPREL1gene causes severe non-syndromic high myopia with early-onset cataract
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Title
Homozygous loss-of-function mutation of theLEPREL1gene causes severe non-syndromic high myopia with early-onset cataract
Authors
Keywords
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Journal
CLINICAL GENETICS
Volume 86, Issue 6, Pages 575-579
Publisher
Wiley
Online
2013-10-30
DOI
10.1111/cge.12309
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Note: Only part of the references are listed.- Mutations in SCO2 Are Associated with Autosomal-Dominant High-Grade Myopia
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- A genome-wide association study reveals association between common variants in an intergenic region of 4q25 and high-grade myopia in the Chinese Han population
- (2011) Zhiqiang Li et al. HUMAN MOLECULAR GENETICS
- A Role for Prolyl 3-Hydroxylase 2 in Post-translational Modification of Fibril-forming Collagens
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- (2009) H. Li et al. BIOINFORMATICS
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- (2009) H. Li et al. BIOINFORMATICS
- Myopia genetics: a review of current research and emerging trends
- (2009) Dana M Hornbeak et al. CURRENT OPINION IN OPHTHALMOLOGY
- A Genome-Wide Association Analysis Identified a Novel Susceptible Locus for Pathological Myopia at 11q24.1
- (2009) Hideo Nakanishi et al. PLoS Genetics
- Effect of the -Gly-3(S)-hydroxyprolyl-4(R)-hydroxyprolyl- tripeptide unit on the stability of collagen model peptides
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- Conservation of notochord gene expression across chordates: Insights from theLeprecangene family
- (2008) Terence D. Capellini et al. GENESIS
- Refractive Errors in an Elderly Japanese Population
- (2008) Akira Sawada et al. OPHTHALMOLOGY
- Prevalence of Myopia in Urban and Rural Children in Mainland China
- (2008) Mingguang He et al. OPTOMETRY AND VISION SCIENCE
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