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Recurrent Rare Copy Number Variants Increase Risk for Esotropia
PURPOSE: To determine whether rare copy number variants (CNVs) increase risk for comitant esotropia. METHODS: CNVs were identified in 1614 Caucasian individuals with comitant esotropia and 3922 Caucasian controls from Illumina SNP genotyping using two Hidden Markov model (HMM) algorithms, PennCNV an...
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| Foilsithe in: | Invest Ophthalmol Vis Sci |
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| Main Authors: | , , , , , , , , , , , , , , , , , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
The Association for Research in Vision and Ophthalmology
2020
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7443120/ https://ncbi.nlm.nih.gov/pubmed/32780866 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.61.10.22 |
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