Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy

D. Lal; H. Trucks; R.S. Moller; H. Hjalgrim; B.P.C. Koeleman; C.G.F. de Kovel; F. Visscher; Y.G. Weber; H. Lerche; F. Becker; C.J. Schankin; B.A. Neubauer; R. Surges; W.S. Kunz; F. Zimprich; A. Franke; T. Illig; J.S. Ried; P. Nürnberg; x EMINet Consortium; x EPICURE Consortium; T. Sander

Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy

Translated title of the contribution: Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy

D. Lal
, H. Trucks
, R.S. Moller
, H. Hjalgrim
, B.P.C. Koeleman
, C.G.F. de Kovel
, F. Visscher
, Y.G. Weber
, H. Lerche
, F. Becker
, C.J. Schankin
, B.A. Neubauer
, R. Surges
, W.S. Kunz
, F. Zimprich
, A. Franke
, T. Illig
, J.S. Ried
, P. Nürnberg
, x EMINet Consortium

x EPICURE Consortium, T. Sander

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

Translated title of the contribution	Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy
Original language	Undefined/Unknown
Pages (from-to)	265-271
Number of pages	7
Journal	Epilepsia
Volume	54
Issue number	2
Publication status	Published - 2013

Keywords

Econometric and Statistical Methods: General
Geneeskunde (GENK)
Geneeskunde(GENK)
Medical sciences
Bescherming en bevordering van de menselijke gezondheid

Access to Document

http://www.ncbi.nlm.nih.gov/pubmed/?term=23350840

Cite this

Lal, D., Trucks, H., Moller, R. S., Hjalgrim, H., Koeleman, B. P. C., de Kovel, C. G. F., Visscher, F., Weber, Y. G., Lerche, H., Becker, F., Schankin, C. J., Neubauer, B. A., Surges, R., Kunz, W. S., Zimprich, F., Franke, A., Illig, T., Ried, J. S., Nürnberg, P., ... Sander, T. (2013). Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy. Epilepsia, 54(2), 265-271. http://www.ncbi.nlm.nih.gov/pubmed/?term=23350840

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title = "Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy",

keywords = "Econometric and Statistical Methods: General, Geneeskunde (GENK), Geneeskunde(GENK), Medical sciences, Bescherming en bevordering van de menselijke gezondheid",

author = "D. Lal and H. Trucks and R.S. Moller and H. Hjalgrim and B.P.C. Koeleman and \{de Kovel\}, C.G.F. and F. Visscher and Y.G. Weber and H. Lerche and F. Becker and C.J. Schankin and B.A. Neubauer and R. Surges and W.S. Kunz and F. Zimprich and A. Franke and T. Illig and J.S. Ried and P. N{\"u}rnberg and \{EMINet Consortium\}, x and \{EPICURE Consortium\}, x and T. Sander",

year = "2013",

language = "Undefined/Unknown",

volume = "54",

pages = "265--271",

journal = "Epilepsia",

issn = "0013-9580",

publisher = "Wiley-Blackwell Publishing Ltd",

number = "2",

}

Lal, D, Trucks, H, Moller, RS, Hjalgrim, H, Koeleman, BPC, de Kovel, CGF, Visscher, F, Weber, YG, Lerche, H, Becker, F, Schankin, CJ, Neubauer, BA, Surges, R, Kunz, WS, Zimprich, F, Franke, A, Illig, T, Ried, JS, Nürnberg, P, EMINet Consortium, X, EPICURE Consortium, X & Sander, T 2013, 'Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy', Epilepsia, vol. 54, no. 2, pp. 265-271. <http://www.ncbi.nlm.nih.gov/pubmed/?term=23350840>

TY - JOUR

T1 - Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy

AU - Lal, D.

AU - Trucks, H.

AU - Moller, R.S.

AU - Hjalgrim, H.

AU - Koeleman, B.P.C.

AU - de Kovel, C.G.F.

AU - Visscher, F.

AU - Weber, Y.G.

AU - Lerche, H.

AU - Becker, F.

AU - Schankin, C.J.

AU - Neubauer, B.A.

AU - Surges, R.

AU - Kunz, W.S.

AU - Zimprich, F.

AU - Franke, A.

AU - Illig, T.

AU - Ried, J.S.

AU - Nürnberg, P.

AU - EMINet Consortium, x

AU - EPICURE Consortium, x

AU - Sander, T.

PY - 2013

Y1 - 2013

KW - Econometric and Statistical Methods: General

KW - Geneeskunde (GENK)

KW - Geneeskunde(GENK)

KW - Medical sciences

KW - Bescherming en bevordering van de menselijke gezondheid

M3 - Article

SN - 0013-9580

VL - 54

SP - 265

EP - 271

JO - Epilepsia

JF - Epilepsia

IS - 2

ER -