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Bi-allelic mutation of CTNNB1 causes a severe form of syndromic microphthalmia, persistent foetal vasculature and vitreoretinal dysplasia. (2022)

First Author: Taylor RL

Attributed to: iPSC modelling and multi-omics analysis to understand age-related macular degeneration funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1186/s13023-022-02239-3

PubMed Identifier: 35246174

Publication URI: http://europepmc.org/abstract/MED/35246174

Type: Journal Article/Review

Volume: 17

Parent Publication: Orphanet journal of rare diseases

Issue: 1

ISSN: 1750-1172