An Unusual Retinal Phenotype Associated With a Mutation in Sterol Carrier Protein SCP2. (2017)
Attributed to:
iPSC modelling and multi-omics analysis to understand age-related macular degeneration
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1001/jamaophthalmol.2016.4985
PubMed Identifier: 28033445
Publication URI: http://europepmc.org/abstract/MED/28033445
Type: Journal Article/Review
Volume: 135
Parent Publication: JAMA ophthalmology
Issue: 2
ISSN: 2168-6165