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. 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

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

NIN

Onderzoeksoutput: Bijdrage aan wetenschappelijk tijdschrift/periodieke uitgave › Artikel › Wetenschappelijk › peer review

Originele taal-2	Engels
Pagina's (van-tot)	1185-1192
Tijdschrift	Human Molecular Genetics
Volume	7
Status	Gepubliceerd - 1998

Citeer dit

Dunnen, J. T. D., Kraayenbrink, T., Schooneveld, M. V., Vosse, E. V. D., de Jong, P. T. V. M., Brink, J. B. T., Schuurman, E., Tijmes, N., Ommen, G. J. B. V., Bergen, A. A. B., Andolfi, G., Montini, E., Li, Y., Oudet, C., Bolz, H., Kaplan, J., Orth, U., Gal, A., Hanauer, A., ... 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.

@article{798326ee1bc549439551656c935c2bc8,

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

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

year = "1998",

language = "English",

volume = "7",

pages = "1185--1192",

journal = "Human Molecular Genetics",

issn = "0964-6906",

publisher = "Oxford University Press",

}

Dunnen, JTD, Kraayenbrink, T, Schooneveld, MV, Vosse, EVD, de Jong, PTVM, Brink, JBT, Schuurman, E, Tijmes, N, Ommen, GJBV, Bergen, AAB, Andolfi, G, Montini, E, Li, Y, Oudet, C, Bolz, H, Kaplan, J, Orth, U, Gal, A, Hanauer, A, Bardelli, AM, Ayuso, C, Diaz, FJ, Bitoun, P, Ventruto, P, Ballabio, A, Franco, B, Hiriyanna, KT, Bingham, EL, Mchenry, C, Pawar, H, Coats, C, Darga, T, Richards, JE, Sieving, PA, Huopaniemi, L, Rantala, A, Rosenberg, T, Dahl, N, Wright, A, Delachapelle, A, Alitalo, O, Lenzner, S, Brunner, B, Feil, S, Niesler, B, Schulz, U, Pinckers, A, Blankennagel, A, Ruether, K, Kellner, U, Rappold, G, Ropers, HH, Kalscheuer, V, Berger, W, Trump, D, Walpole, SM, Nicolaou, A, Gaythor, SA, Pimenides, D, George, NDL, Moore, UT & Yates, JRW 1998, 'Functional implications of the spectrum of mutations found in 234 cases with X-linked juvenile retinoschisis (XLRS)', Human Molecular Genetics, vol. 7, blz. 1185-1192.

TY - JOUR

T1 - Functional implications of the spectrum of mutations found in 234 cases with X-linked juvenile retinoschisis (XLRS)

AU - Dunnen, J.T. den

AU - Kraayenbrink, T.

AU - Schooneveld, M. van

AU - Vosse, E. van de

AU - de Jong, P.T.V.M.

AU - Brink, J.B. ten

AU - Schuurman, E.

AU - Tijmes, N.

AU - Ommen, G.J.B. van

AU - Bergen, A.A.B.

AU - Andolfi, G.

AU - Montini, E.

AU - Li, Y.

AU - Oudet, C.

AU - Bolz, H.

AU - Kaplan, J.

AU - Orth, U.

AU - Gal, A.

AU - Hanauer, A.

AU - Bardelli, A.M.

AU - Ayuso, C.

AU - Diaz, F.J.

AU - Bitoun, P.

AU - Ventruto, P.

AU - Ballabio, A.

AU - Franco, B.

AU - Hiriyanna, K.T.

AU - Bingham, E.L.

AU - Mchenry, C.

AU - Pawar, H.

AU - Coats, C.

AU - Darga, T.

AU - Richards, J.E.

AU - Sieving, P.A.

AU - Huopaniemi, L.

AU - Rantala, A.

AU - Rosenberg, T.

AU - Dahl, N.

AU - Wright, A.

AU - Delachapelle, A.

AU - Alitalo, O.

AU - Lenzner, S.

AU - Brunner, B.

AU - Feil, S.

AU - Niesler, B.

AU - Schulz, U.

AU - Pinckers, A.

AU - Blankennagel, A.

AU - Ruether, K.

AU - Kellner, U.

AU - Rappold, G.

AU - Ropers, H.H.

AU - Kalscheuer, V.

AU - Berger, W.

AU - Trump, D.

AU - Walpole, S.M.

AU - Nicolaou, A.

AU - Gaythor, S.A.

AU - Pimenides, D.

AU - George, N.D.L.

AU - Moore, U.T.

AU - Yates, J.R.W.

PY - 1998

Y1 - 1998

M3 - Article

SN - 0964-6906

VL - 7

SP - 1185

EP - 1192

JO - Human Molecular Genetics

JF - Human Molecular Genetics

ER -