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Developing gene therapy for inherited retinal degenerations (2022)

First Author: Yusuf I

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/10.5287/ora-7ryp2xvmj

Publication URI: https://ora.ox.ac.uk/objects/uuid:41a85db2-d906-4099-8ba0-69c337e30db4

Type: Thesis