Association analyses of rare variants identify two genes associated with refractive error

PURPOSE: Genetic variants identified through population-based genome-wide studies are generally of high frequency, exerting their action in the central part of the refractive error spectrum. However, the power to identify associations with variants of lower minor allele frequency is greatly reduced,...

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Detalles Bibliográficos
Autores principales: Patasova, Karina, Haarman, Annechien E. G., Musolf, Anthony M., Mahroo, Omar A., Rahi, Jugnoo S., Falchi, Mario, Verhoeven, Virginie J. M., Bailey-Wilson, Joan E., Klaver, Caroline C. W., Duggal, Priya, Klein, Alison, Guggenheim, Jeremy A., Hammond, Chris J., Hysi, Pirro G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9499304/
https://www.ncbi.nlm.nih.gov/pubmed/36137074
http://dx.doi.org/10.1371/journal.pone.0272379

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9499304/
https://www.ncbi.nlm.nih.gov/pubmed/36137074
http://dx.doi.org/10.1371/journal.pone.0272379

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