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

Dunnen, J.T. den and Kraayenbrink, T. and Schooneveld, M. van and Vosse, E. van de and Jong de, P.T.V.M. and Brink, J.B. ten and Schuurman, E. and Tijmes, N. and Ommen, G.J.B. van and Bergen, A.A.B. and Andolfi, G. and Montini, E. and Li, Y. and Oudet, C. and Bolz, H. and Kaplan, J. and Orth, U. and Gal, A. and Hanauer, A. and Bardelli, A.M. and Ayuso, C. and Diaz, F.J. and Bitoun, P. and Ventruto, P. and Ballabio, A. and Franco, B. and Hiriyanna, K.T. and Bingham, E.L. and Mchenry, C. and Pawar, H. and Coats, C. and Darga, T. and Richards, J.E. and Sieving, P.A. and Huopaniemi, L. and Rantala, A. and Rosenberg, T. and Dahl, N. and Wright, A. and Delachapelle, A. and Alitalo, O. and Lenzner, S. and Brunner, B. and Feil, S. and Niesler, B. and Schulz, U. and Pinckers, A. and Blankennagel, A. and Ruether, K. and Kellner, U. and Rappold, G. and Ropers, H.H. and Kalscheuer, V. and Berger, W. and Trump, D. and Walpole, S.M. and Nicolaou, A. and Gaythor, S.A. and Pimenides, D. and George, N.D.L. and Moore, U.T. and Yates, J.R.W. (1998) Functional implications of the spectrum of mutations found in 234 cases with X-linked juvenile retinoschisis (XLRS). Human molecular genetics, 7, 1185-1192. ISSN 09646906.

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Item Type:Article
Institutes:Netherlands Institute for Neuroscience (NIN)
ID Code:1659
Deposited On:13 Feb 2009 16:59
Last Modified:10 Dec 2009 13:14

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