📣 Help Shape the Future of UKRI's Gateway to Research (GtR)

We're improving UKRI's Gateway to Research and are seeking your input! If you would be interested in being interviewed about the improvements we're making and to have your say about how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community, please email gateway@ukri.org.

SLC38A8 mutations result in arrested retinal development with loss of cone photoreceptor specialization (2020)

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