|
Literature for OMIM 610356: RETINAL CONE DYSTROPHY 3B; RCD3B
Xenbase Articles:
( Denotes literature images)
Functional analysis of missense mutations in Kv8.2 causing cone dystrophy with supernormal rod electroretinogram., Smith KE,Wilkie SE,Tebbs-Warner JT,Jarvis BJ,Gallasch L,Stocker M,Hunt DM, J Biol Chem. December 21, 2012; 287(52):1083-351X. |