B. Jeroen Klevering
Department of Ophthalmology
University Medical Centre Nijmegen
PO Box 9101
6500 HB Nijmegen
Netherlands
Name/email consistency: high
- The spectrum of retinal phenotypes caused by mutations in the ABCA4 gene. Klevering, B.J., Deutman, A.F., Maugeri, A., Cremers, F.P., Hoyng, C.B. Graefes Arch. Clin. Exp. Ophthalmol. (2005)
- Three families displaying the combination of Stargardt's disease with cone-rod dystrophy or retinitis pigmentosa. Klevering, B.J., Maugeri, A., Wagner, A., Go, S.L., Vink, C., Cremers, F.P., Hoyng, C.B. Ophthalmology (2004)