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. Zobor; A. Bernd; B.P. Leroy; P. Enyedi; F.P. Cremers; B. Lorenz; E. Zrenner; S. Kohl

doi:10.1002/humu.21580

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

Netherlands Institute for Neuroscience (NIN)

Research output: Contribution to journal/periodical › Article › Scientific › peer-review

Original language	English
Pages (from-to)	1398-1406
Journal	Human Mutation
Volume	32
DOIs	https://doi.org/10.1002/humu.21580
Publication status	Published - 2011

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10.1002/humu.21580

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Wissinger, B., Schaich, S., Baumann, B., Bonin, M., Jagle, H., Friedburg, C., Varsanyi, B., Hoyng, C. B., Dolfus, H., Heckenlively, J. R., Rosenberg, T., Rudolph, G., Kellner, U., Salati, R., Plomp, A. S., De Baere, E., Andrassi-Darida, M., Sauer, A., Wolf, C., ... Kohl, S. (2011). Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response. Human Mutation, 32, 1398-1406. https://doi.org/10.1002/humu.21580

Wissinger, B. ; Schaich, S. ; Baumann, B. ; Bonin, M. ; Jagle, H. ; Friedburg, C. ; Varsanyi, B. ; Hoyng, C.B. ; Dolfus, H. ; Heckenlively, J.R. ; Rosenberg, T. ; Rudolph, G. ; Kellner, U. ; Salati, R. ; Plomp, A.S. ; De Baere, E. ; Andrassi-Darida, M. ; Sauer, A. ; Wolf, C. ; Zobor, D. ; Bernd, A. ; Leroy, B.P. ; Enyedi, P. ; Cremers, F.P. ; Lorenz, B. ; Zrenner, E. ; Kohl, S. / Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response. In: Human Mutation. 2011 ; Vol. 32. pp. 1398-1406.

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

author = "B. Wissinger and S. Schaich and B. Baumann and M. Bonin and H. Jagle and C. Friedburg and B. Varsanyi and C.B. Hoyng and H. Dolfus and J.R. Heckenlively and T. Rosenberg and G. Rudolph and U. Kellner and R. Salati and A.S. Plomp and {De Baere}, E. and M. Andrassi-Darida and A. Sauer and C. Wolf and D. Zobor and A. Bernd and B.P. Leroy and P. Enyedi and F.P. Cremers and B. Lorenz and E. Zrenner and S. Kohl",

note = "Reporting year: 2011",

year = "2011",

doi = "10.1002/humu.21580",

language = "English",

volume = "32",

pages = "1398--1406",

journal = "Human Mutation",

issn = "1059-7794",

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Wissinger, B, Schaich, S, Baumann, B, Bonin, M, Jagle, H, Friedburg, C, Varsanyi, B, Hoyng, CB, Dolfus, H, Heckenlively, JR, Rosenberg, T, Rudolph, G, Kellner, U, Salati, R, Plomp, AS, De Baere, E, Andrassi-Darida, M, Sauer, A, Wolf, C, Zobor, D, Bernd, A, Leroy, BP, Enyedi, P, Cremers, FP, Lorenz, B, Zrenner, E & Kohl, S 2011, 'Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response.', Human Mutation, vol. 32, pp. 1398-1406. https://doi.org/10.1002/humu.21580

Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response. / Wissinger, B.; Schaich, S.; Baumann, B.; Bonin, M.; Jagle, H.; Friedburg, C.; Varsanyi, B.; Hoyng, C.B.; Dolfus, H.; Heckenlively, J.R.; Rosenberg, T.; Rudolph, G.; Kellner, U.; Salati, R.; Plomp, A.S.; De Baere, E.; Andrassi-Darida, M.; Sauer, A.; Wolf, C.; Zobor, D.; Bernd, A.; Leroy, B.P.; Enyedi, P.; Cremers, F.P.; Lorenz, B.; Zrenner, E.; Kohl, S.

In: Human Mutation, Vol. 32, 2011, p. 1398-1406.

Research output: Contribution to journal/periodical › Article › Scientific › peer-review

TY - JOUR

T1 - Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response.

AU - Wissinger, B.

AU - Schaich, S.

AU - Baumann, B.

AU - Bonin, M.

AU - Jagle, H.

AU - Friedburg, C.

AU - Varsanyi, B.

AU - Hoyng, C.B.

AU - Dolfus, H.

AU - Heckenlively, J.R.

AU - Rosenberg, T.

AU - Rudolph, G.

AU - Kellner, U.

AU - Salati, R.

AU - Plomp, A.S.

AU - De Baere, E.

AU - Andrassi-Darida, M.

AU - Sauer, A.

AU - Wolf, C.

AU - Zobor, D.

AU - Bernd, A.

AU - Leroy, B.P.

AU - Enyedi, P.

AU - Cremers, F.P.

AU - Lorenz, B.

AU - Zrenner, E.

AU - Kohl, S.

N1 - Reporting year: 2011

PY - 2011

Y1 - 2011

U2 - 10.1002/humu.21580

DO - 10.1002/humu.21580

M3 - Article

VL - 32

SP - 1398

EP - 1406

JO - Human Mutation

JF - Human Mutation

SN - 1059-7794

ER -