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...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Invest Ophthalmol Vis Sci
Main Authors: Whitman, Mary C., Di Gioia, Silvio Alessandro, Chan, Wai-Man, Gelber, Alon, Pratt, Brandon M., Bell, Jessica L., Collins, Thomas E., Knowles, James A., Armoskus, Christopher, Pato, Michele, Pato, Carlos, Shaaban, Sherin, Staffieri, Sandra, MacKinnon, Sarah, Maconachie, Gail D E., Elder, James E., Traboulsi, Elias I., Gottlob, Irene, Mackey, David A., Hunter, David G., Engle, Elizabeth C.
Formato: Artigo
Idioma:Inglês
Publicado em: The Association for Research in Vision and Ophthalmology 2020
Assuntos:
Eye Movements, Strabismus, Amblyopia and Neuro-Ophthalmology
Acesso em linha: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
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados