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An Unusual Retinal Phenotype Associated With a Mutation in Sterol Carrier Protein SCP2. (2017)

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