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XB-GENEPAGE-940168
Papers associated with kcnv2
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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): 43972-83. |
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Characterization of the heteromeric potassium channel formed by kv2.1 and the retinal subunit kv8.2 in Xenopus oocytes., Czirjak G, Toth ZE, Enyedi P., J Neurophysiol. September 1, 2007; 98 (3): 1213-22. |
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