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Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response.

Publication year 2011
Published in Human Mutation
Authors B. Wissinger, S. Schaich, B. Baumann, M. Bonin, H. Jagle, C. Friedburg, B. Varsanyi, C.B. Hoyng, H. Dolfus, J.R. Heckenlively, T. Rosenberg, G. Rudolph, U. Kellner, R. Salati, A.S. Plomp, E. De Baere, M. Andrassi-Darida, A. Sauer, C. Wolf, D. Zobor, A. Bernd, B.P. Leroy, P. Enyedi, F.P. Cremers, B. Lorenz, E. Zrenner, S. Kohl

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