A splice-site variant in FLVCR1 produces retinitis pigmentosa without posterior column ataxia. (2018)

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/10.1080/13816810.2017.1408848

PubMed Identifier: 29192808

Publication URI: http://europepmc.org/abstract/MED/29192808

Type: Journal Article/Review

Volume: 39

Parent Publication: Ophthalmic genetics

Issue: 2

ISSN: 1381-6810