A novel splice-site variant in CDH23 in a patient with Usher syndrome type 1. (2019)

First Author: Menghini M
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/10.1080/13816810.2019.1692359

PubMed Identifier: 31755791

Publication URI: http://europepmc.org/abstract/MED/31755791

Type: Journal Article/Review

Volume: 40

Parent Publication: Ophthalmic genetics

Issue: 6

ISSN: 1381-6810