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Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism. (2008)

First Author: Jacobson SG

Attributed to: GRL - Prof Steel funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/hmg/ddn140

PubMed Identifier: 18463160

Publication URI: http://europepmc.org/abstract/MED/18463160

Type: Journal Article/Review

Volume: 17

Parent Publication: Human molecular genetics

Issue: 15

ISSN: 0964-6906