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

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. ZoborA. Bernd, B.P. Leroy, P. Enyedi, F.P. Cremers, B. Lorenz, E. Zrenner, S. Kohl

Research output: Contribution to journal/periodicalArticleScientificpeer-review

Original languageEnglish
Pages (from-to)1398-1406
JournalHuman Mutation
Publication statusPublished - 2011

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