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