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