Gene Therapy Targeting the Inner Retina Rescues the Retinal Phenotype in a Mouse Model of CLN3 Batten Disease. (2020)
Attributed to:
The development of gene therapy for infantile neuroaxonal dystrophy
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1089/hum.2020.038
PubMed Identifier: 32578444
Publication URI: http://europepmc.org/abstract/MED/32578444
Type: Journal Article/Review
Volume: 31
Parent Publication: Human gene therapy
Issue: 13-14
ISSN: 1043-0342