Leber congenital amaurosis and retinitis pigmentosa with coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (crb1) gene

A.I. den Hollander; J.R. Heckenlively; L.I. van den Born; Y.J.M. de Kok; S.D. van der Velde-Visser; U Kellner; B Jurklies; M.J. van Schooneveld; A Blankenagel; K Rohrschneider; B Wissinger; J.R.M. Cruysberg; A.F. Deutman; H.G. Brunner; E Apfelstedt-sylla; C.B. Hoyng; F.P.M. Cremers

Leber congenital amaurosis and retinitis pigmentosa with coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (crb1) gene

Translated title of the contribution: Leber congenital amaurosis and retinitis pigmentosa with coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (crb1) gene

A.I. den Hollander, J.R. Heckenlively, L.I. van den Born, Y.J.M. de Kok, S.D. van der Velde-Visser, U Kellner, B Jurklies, M.J. van Schooneveld, A Blankenagel, K Rohrschneider, B Wissinger, J.R.M. Cruysberg, A.F. Deutman, H.G. Brunner, E Apfelstedt-sylla, C.B. Hoyng, F.P.M. Cremers

Department of Ophthalmology

Research output: Contribution to journal › Article › Academic › peer-review

Translated title of the contribution	Leber congenital amaurosis and retinitis pigmentosa with coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (crb1) gene
Original language	Undefined/Unknown
Pages (from-to)	198-203
Number of pages	6
Journal	American Journal of Human Genetics
Volume	69
Publication status	Published - 2001

Keywords

Econometric and Statistical Methods: General
Geneeskunde (GENK)
Geneeskunde(GENK)
Algemeen onderzoek
Other medical specialities

Cite this

den Hollander, A. I., Heckenlively, J. R., van den Born, L. I., de Kok, Y. J. M., van der Velde-Visser, S. D., Kellner, U., Jurklies, B., van Schooneveld, M. J., Blankenagel, A., Rohrschneider, K., Wissinger, B., Cruysberg, J. R. M., Deutman, A. F., Brunner, H. G., Apfelstedt-sylla, E., Hoyng, C. B., & Cremers, F. P. M. (2001). Leber congenital amaurosis and retinitis pigmentosa with coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (crb1) gene. American Journal of Human Genetics, 69, 198-203.

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title = "Leber congenital amaurosis and retinitis pigmentosa with coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (crb1) gene",

keywords = "Econometric and Statistical Methods: General, Geneeskunde (GENK), Geneeskunde(GENK), Algemeen onderzoek, Other medical specialities",

author = "{den Hollander}, A.I. and J.R. Heckenlively and {van den Born}, L.I. and {de Kok}, Y.J.M. and {van der Velde-Visser}, S.D. and U Kellner and B Jurklies and {van Schooneveld}, M.J. and A Blankenagel and K Rohrschneider and B Wissinger and J.R.M. Cruysberg and A.F. Deutman and H.G. Brunner and E Apfelstedt-sylla and C.B. Hoyng and F.P.M. Cremers",

year = "2001",

language = "Undefined/Unknown",

volume = "69",

pages = "198--203",

journal = "American Journal of Human Genetics",

issn = "0002-9297",

publisher = "Cell Press",

}

den Hollander, AI, Heckenlively, JR, van den Born, LI, de Kok, YJM, van der Velde-Visser, SD, Kellner, U, Jurklies, B, van Schooneveld, MJ, Blankenagel, A, Rohrschneider, K, Wissinger, B, Cruysberg, JRM, Deutman, AF, Brunner, HG, Apfelstedt-sylla, E, Hoyng, CB & Cremers, FPM 2001, 'Leber congenital amaurosis and retinitis pigmentosa with coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (crb1) gene', American Journal of Human Genetics, vol. 69, pp. 198-203.

Leber congenital amaurosis and retinitis pigmentosa with coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (crb1) gene. / den Hollander, A.I.; Heckenlively, J.R.; van den Born, L.I. et al.
In: American Journal of Human Genetics, Vol. 69, 2001, p. 198-203.

Research output: Contribution to journal › Article › Academic › peer-review

TY - JOUR

T1 - Leber congenital amaurosis and retinitis pigmentosa with coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (crb1) gene

AU - den Hollander, A.I.

AU - Heckenlively, J.R.

AU - van den Born, L.I.

AU - de Kok, Y.J.M.

AU - van der Velde-Visser, S.D.

AU - Kellner, U

AU - Jurklies, B

AU - van Schooneveld, M.J.

AU - Blankenagel, A

AU - Rohrschneider, K

AU - Wissinger, B

AU - Cruysberg, J.R.M.

AU - Deutman, A.F.

AU - Brunner, H.G.

AU - Apfelstedt-sylla, E

AU - Hoyng, C.B.

AU - Cremers, F.P.M.

PY - 2001

Y1 - 2001

KW - Econometric and Statistical Methods: General

KW - Geneeskunde (GENK)

KW - Geneeskunde(GENK)

KW - Algemeen onderzoek

KW - Other medical specialities

M3 - Article

SN - 0002-9297

VL - 69

SP - 198

EP - 203

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

ER -