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

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Publication year
1998
Author(s)
Dendunnen, J.T.
Kraayenbrink, T.
Schooneveld, M. van
Vosse, E. van de
Jong, P.T.V.M. de
Brink, J.B. ten
Schuurman, E.J.M.
Tijmes, N.
Ommen, G.J.B. van
Bergen, A.A.B.
Andolfi, G.
Montini, E.
Oudet, C.
Bolz, H.
Kaplan, J.
Orth, U.
Gal, A.
Hanauer, A.
Bardelli, A.M.
Ayuso, C.
Diaz, F.J.
Bitoun, P.
Ventruto, V.
Ballabio, A.
Franco, B.
Hiriyana, K.T.
Bingham, E.L.
McHenry, C.
Pawar, H.
Coats, C.
Darga, T.
Richards, J.E.
Sieving, P.A.
Huopaniemi, L.
Rantala, A.
Rosenberg, T.
Dahl, N.
Wright, A.
Chapelle, A. dela
Alitalo, T.
Lenzner, S.
Brunner, H.G.
Feil, S.
Niesler, B.
Schulz, U.
Pinckers, A.J.L.G.
Blankenagel, A.
Ruether, K.
Kellner, U.
Rappold, G.A.
Ropers, H.H.
Kalscheuer, V.M.M.
Berger, W.
Trump, D.
Walpole, S.M.
Nicolaou, A.
Gaythor, S.A.
Pimenides, D.
George, N.D.L.
Moore, U.T.
Yates, J.R.W.
Number of pages
8 p.
Source
Human Molecular Genetics, 7, (1998), pp. 1185-1192
ISSN
Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/189361   https://hdl.handle.net/2066/189361
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