Functional analysis of missense mutations in Kv8.2 causing cone dystrophy with supernormal rod electroretinogram. (2012)
Attributed to:
A study of the role of Kv8.2 a novel potassium channel gene in retinal physiology and phototransduction
funded by
BBSRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1074/jbc.m112.388033
PubMed Identifier: 23115240
Publication URI: http://europepmc.org/abstract/MED/23115240
Type: Journal Article/Review
Volume: 287
Parent Publication: The Journal of biological chemistry
Issue: 52
ISSN: 0021-9258