SLC38A8 mutations result in arrested retinal development with loss of cone photoreceptor specialization (2020)
Attributed to:
Driving innovation in precision medicine through translational life sciences research at the University of Leicester
funded by
UKRI
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/hmg/ddaa166
PubMed Identifier: 32744312
Publication URI: http://europepmc.org/abstract/MED/32744312
Type: Journal Article/Review
Parent Publication: Human Molecular Genetics
Issue: 18
ISSN: 0964-6906