Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance

L.M. Dibbens; S. Mullen; I. Helbig; x EPICURE Consortium; D. Kasteleijn-Nolst Trenité; B.P.C. Koeleman; E.H. Brilstra; C.G.F. de Kovel; M.E.M. Swinkels; D. Lindhout; X et al.

Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance

Translated title of the contribution: Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance

L.M. Dibbens
, S. Mullen
, I. Helbig
, x EPICURE Consortium
, D. Kasteleijn-Nolst Trenité
, B.P.C. Koeleman
, E.H. Brilstra
, C.G.F. de Kovel
, M.E.M. Swinkels
, D. Lindhout
, X et al.

Department of Genetics

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

Translated title of the contribution	Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance
Original language	Undefined/Unknown
Pages (from-to)	3626-3631
Number of pages	6
Journal	Human Molecular Genetics
Volume	18
Issue number	19
Publication status	Published - 2009

Keywords

Econometric and Statistical Methods: General
Geneeskunde(GENK)

Cite this

Dibbens, L. M., Mullen, S., Helbig, I., EPICURE Consortium, X., Kasteleijn-Nolst Trenité, D., Koeleman, B. P. C., Brilstra, E. H., de Kovel, C. G. F., Swinkels, M. E. M., Lindhout, D., & et al., X. (2009). Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance. Human Molecular Genetics, 18(19), 3626-3631.

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keywords = "Econometric and Statistical Methods: General, Geneeskunde(GENK)",

author = "L.M. Dibbens and S. Mullen and I. Helbig and \{EPICURE Consortium\}, x and \{Kasteleijn-Nolst Trenit{\'e}\}, D. and B.P.C. Koeleman and E.H. Brilstra and \{de Kovel\}, C.G.F. and M.E.M. Swinkels and D. Lindhout and \{et al.\}, X",

year = "2009",

language = "Undefined/Unknown",

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journal = "Human Molecular Genetics",

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T1 - Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance

AU - Dibbens, L.M.

AU - Mullen, S.

AU - Helbig, I.

AU - EPICURE Consortium, x

AU - Kasteleijn-Nolst Trenité, D.

AU - Koeleman, B.P.C.

AU - Brilstra, E.H.

AU - de Kovel, C.G.F.

AU - Swinkels, M.E.M.

AU - Lindhout, D.

AU - et al., X

PY - 2009

Y1 - 2009

KW - Econometric and Statistical Methods: General

KW - Geneeskunde(GENK)

M3 - Article

SN - 0964-6906

VL - 18

SP - 3626

EP - 3631

JO - Human Molecular Genetics

JF - Human Molecular Genetics

IS - 19

ER -