Rare disease gene association discovery from burden analysis of the 100,000 Genomes Project data. (2023)
Attributed to:
Gene regulation, genetic mechanisms and development of potential therapies for corneal endothelial dystrophies
funded by
FLF
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1101/2023.12.20.23300294
PubMed Identifier: 38196618
Publication URI: http://europepmc.org/abstract/MED/38196618
Type: Journal Article/Review
Parent Publication: medRxiv : the preprint server for health sciences