Missense variants in the X-linked gene PRPS1 cause retinal degeneration in females. (2018)
Attributed to:
Understanding the mechanisms of cone opsin mediated disease to develop new therapies
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1002/humu.23349
PubMed Identifier: 28967191
Publication URI: http://europepmc.org/abstract/MED/28967191
Type: Journal Article/Review
Volume: 39
Parent Publication: Human mutation
Issue: 1
ISSN: 1059-7794