CFH Haploinsufficiency and Complement Alterations in Early-Onset Macular Degeneration-Reference-Cited by-同舟云学术

CFH Haploinsufficiency and Complement Alterations in Early-Onset Macular Degeneration

Published:2024-04-29 Issue:4 Volume:65 Page:43
ISSN:1552-5783
Container-title:Investigative Ophthalmology & Visual Science
language:en
Short-container-title:Invest. Ophthalmol. Vis. Sci.

Author:

Lim Rayne R.¹,Shirali Sharlene¹,Rowlan Jessica¹,Engel Abbi L.²,Nazario, Marcos¹,Gonzalez Kelie¹,Tong Aspen¹,Neitz Jay¹,Neitz Maureen¹,Chao Jennifer R.¹³

Affiliation:

1. Department of Ophthalmology, University of Washington, Seattle, Washington, United States

2. Center for Developmental Biology and Regenerative Medicine, Seattle Children's Institute, Seattle, Washington, United States

3. Roger and Angie Karalis Johnson Retina Center, University of Washington School of Medicine, Seattle, Washington, United States

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Reference52 articles.

1. Global prevalence of age-related macular degeneration and disease burden projection for 2020 and 2040: a systematic review and meta-analysis;Wong;Lancet Glob Health,2014

2. Complement activation and inhibition in retinal diseases;Kleinman;Dev Ophthalmol,2016

3. A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degeneration;Hageman;Proc Natl Acad Sci USA,2005

4. Polymorphisms in C2, CFB and C3 are associated with progression to advanced age related macular degeneration associated with visual loss;Francis;J Med Genet,2009

5. Complement factor H in AMD: bridging genetic associations and pathobiology;Toomey;Prog Retin Eye Res,2018

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