Phenotypic Expression of CFH Rare Variants in Age-Related Macular Degeneration Patients in the Coimbra Eye Study

PURPOSE: To determine the association between rare genetic variants in complement factor H (CFH) and phenotypic features in age-related macular degeneration (AMD) patients from the Coimbra Eye Study (CES). METHODS: AMD patients from the Incidence CES (NCT02748824) underwent ophthalmologic examinatio...

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Detalles Bibliográficos
Autores principales: Farinha, Cláudia, Barreto, Patrícia, Coimbra, Rita, Iutis, Adela, Cachulo, Maria Luz, Cunha-Vaz, José, Lechanteur, Yara T. E., Hoyng, Carel B., Silva, Rufino
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2022
Materias:
Retina
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9363674/
https://www.ncbi.nlm.nih.gov/pubmed/35925583
http://dx.doi.org/10.1167/iovs.63.9.5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9363674/
https://www.ncbi.nlm.nih.gov/pubmed/35925583
http://dx.doi.org/10.1167/iovs.63.9.5

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