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Deep phenotyping of the Cdhr1-/- mouse validates its use in pre-clinical studies for human CDHR1-associated retinal degeneration. (2021)

First Author: Yusuf IH

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/10.1016/j.exer.2021.108603

PubMed Identifier: 33964272

Publication URI: http://europepmc.org/abstract/MED/33964272

Type: Journal Article/Review

Volume: 208

Parent Publication: Experimental eye research

ISSN: 0014-4835