Clinical Characterization of Retinitis Pigmentosa Associated With Variants in SNRNP200. (2019)
Attributed to:
Development of AAV gene therapy for blindness caused by cone-rod dystrophy
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1001/jamaophthalmol.2019.3298
PubMed Identifier: 31486839
Publication URI: http://europepmc.org/abstract/MED/31486839
Type: Journal Article/Review
Volume: 137
Parent Publication: JAMA ophthalmology
Issue: 11
ISSN: 2168-6165