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The role of complement factor I rare genetic variants in age related macular degeneration in Finland. (2025)

First Author: Andreadi A
Attributed to:  Personalised management of atypical haemolytic uraemic syndrome funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/hmg/ddae165

PubMed Identifier: 39584280

Publication URI: http://europepmc.org/abstract/MED/39584280

Type: Journal Article/Review

Volume: 34

Parent Publication: Human molecular genetics

Issue: 3

ISSN: 0964-6906