Functional implications of the spectrum of mutations found in 234 cases with X-linked juvenile retinoschisis (XLRS)

J.T. den Dunnen, T. Kraayenbrink, M. van Schooneveld, E. van de Vosse, P.T.V.M. de Jong, J.B. ten Brink, E. Schuurman, N. Tijmes, G.J.B. van Ommen, A.A.B. Bergen, G. Andolfi, E. Montini, Y. Li, C. Oudet, H. Bolz, J. Kaplan, U. Orth, A. Gal, A. Hanauer, A.M. BardelliC. Ayuso, F.J. Diaz, P. Bitoun, P. Ventruto, A. Ballabio, B. Franco, K.T. Hiriyanna, E.L. Bingham, C. Mchenry, H. Pawar, C. Coats, T. Darga, J.E. Richards, P.A. Sieving, L. Huopaniemi, A. Rantala, T. Rosenberg, N. Dahl, A. Wright, A. Delachapelle, O. Alitalo, S. Lenzner, B. Brunner, S. Feil, B. Niesler, U. Schulz, A. Pinckers, A. Blankennagel, K. Ruether, U. Kellner, G. Rappold, H.H. Ropers, V. Kalscheuer, W. Berger, D. Trump, S.M. Walpole, A. Nicolaou, S.A. Gaythor, D. Pimenides, N.D.L. George, U.T. Moore, J.R.W. Yates

Research output: Contribution to journal/periodicalArticleScientificpeer-review

200 Citations (Scopus)
Original languageEnglish
Pages (from-to)1185-1192
JournalHuman Molecular Genetics
Volume7
Publication statusPublished - 1998

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