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Dive into the research topics of 'Functional analysis of missense mutations in Kv8.2 causing cone dystrophy with supernormal rod electroretinogram'. Together they form a unique fingerprint.- Sort by
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K.E. Smith, S.E. Wilkie, J.T. Tebbs-Warner, B.J. Jarvis, L. Gallasch, M. Stocker, David Hunt
Research output: Contribution to journal › Article › peer-review