A detailed clinical and molecular survey of subjects with nonsyndromic USH2A retinopathy reveals an allelic hierarchy of disease-causing variants. (2015)

First Author: Lenassi E

Attributed to: GRL - Prof Steel funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/ejhg.2014.283

PubMed Identifier: 25649381

Publication URI: http://europepmc.org/abstract/MED/25649381

Type: Journal Article/Review

Volume: 23

Parent Publication: European journal of human genetics : EJHG

Issue: 10

ISSN: 1018-4813