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

Publication year 1998
Published in Human Molecular Genetics
Authors P.T.V.M. de Jong, A.A.B. Bergen, J.T. den Dunnen, T. Kraayenbrink, M. van Schooneveld, E. van de Vosse, J.B. ten Brink, E. Schuurman, N. Tijmes, G.J.B. van Ommen, G. Andolfi, E. Montini, Y. Li, C. Oudet, H. Bolz, J. Kaplan, U. Orth, A. Gal, A. Hanauer, A.M. Bardelli, C. 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,

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