SLC38A8 mutations result in arrested retinal development with loss of cone photoreceptor specialization. (2020)
Abstract
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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
Volume: 29
Parent Publication: Human molecular genetics
Issue: 18
ISSN: 0964-6906