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Dive into the research topics of 'X-linked cone dystrophy and colour vision deficiency arising from a missense mutation in a hybrid L/M cone opsin gene'. Together they form a unique fingerprint.- Sort by
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M.E. Mcclements, Wayne Davies, M. Michaelides, J.D. Carroll, J. Rha, J.D. Mollon, M. Neitz, R.E. Maclaren, A.T. Moore, David Hunt
Research output: Contribution to journal › Article › peer-review