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An assessment of prevalence of Type 1 CFI rare variants in European AMD, and why lack of broader genetic data hinders development of new treatments and healthcare access. (2022)

First Author: Jones AV

Attributed to: UK Biobank (core renewal) funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1371/journal.pone.0272260

PubMed Identifier: 36067162

Publication URI: http://europepmc.org/abstract/MED/36067162

Type: Journal Article/Review

Volume: 17

Parent Publication: PloS one

Issue: 9

ISSN: 1932-6203