Autosomal dominant epilepsy with auditory features: a new LGI1 family including a phenocopy with cortical dysplasia

Karl Martin Klein; Manuela Pendziwiat; Rony Cohen; Silke Appenzeller; Carolien G.F. de Kovel; Felix Rosenow; Bobby P.C. Koeleman; Gregor Kuhlenbäumer; Liron Sheintuch; Ronel Veksler; Alon Friedman; Zaid Afawi; Ingo Helbig

doi:10.1007/s00415-015-7921-2

Autosomal dominant epilepsy with auditory features: a new LGI1 family including a phenocopy with cortical dysplasia

Karl Martin Klein, Manuela Pendziwiat, Rony Cohen, Silke Appenzeller, Carolien G.F. de Kovel, Felix Rosenow, Bobby P.C. Koeleman, Gregor Kuhlenbäumer, Liron Sheintuch, Ronel Veksler, Alon Friedman, Zaid Afawi, Ingo Helbig

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

12 Citations (Scopus)

Original language	English
Pages (from-to)	11-16
Number of pages	6
Journal	Journal of Neurology
Volume	263
Issue number	1
DOIs	https://doi.org/10.1007/s00415-015-7921-2
Publication status	Published - Jan 1 2016
Externally published	Yes

ASJC Scopus Subject Areas

Neurology
Clinical Neurology

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Klein, K. M., Pendziwiat, M., Cohen, R., Appenzeller, S., de Kovel, C. G. F., Rosenow, F., Koeleman, B. P. C., Kuhlenbäumer, G., Sheintuch, L., Veksler, R., Friedman, A., Afawi, Z., & Helbig, I. (2016). Autosomal dominant epilepsy with auditory features: a new LGI1 family including a phenocopy with cortical dysplasia. Journal of Neurology, 263(1), 11-16. https://doi.org/10.1007/s00415-015-7921-2

Klein, KM, Pendziwiat, M, Cohen, R, Appenzeller, S, de Kovel, CGF, Rosenow, F, Koeleman, BPC, Kuhlenbäumer, G, Sheintuch, L, Veksler, R, Friedman, A, Afawi, Z & Helbig, I 2016, 'Autosomal dominant epilepsy with auditory features: a new LGI1 family including a phenocopy with cortical dysplasia', Journal of Neurology, vol. 263, no. 1, pp. 11-16. https://doi.org/10.1007/s00415-015-7921-2

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author = "Klein, {Karl Martin} and Manuela Pendziwiat and Rony Cohen and Silke Appenzeller and {de Kovel}, {Carolien G.F.} and Felix Rosenow and Koeleman, {Bobby P.C.} and Gregor Kuhlenb{\"a}umer and Liron Sheintuch and Ronel Veksler and Alon Friedman and Zaid Afawi and Ingo Helbig",

note = "Funding Information: We thank the family for participation in our study. We also thank the Exome Aggregation Consortium and the groups that provided exome variant data for comparison. A full list of contributing groups can be found at http://exac.broadinstitute.org/about . The study was supported by the Deutsche Forschungsgemeinschaft with a Trilateral Grant (HE 5415/5-1) and within the EuroEPINOMICS project (HE 5415/3-1), the Christian-Albrechts-University Kiel and the Philipps-University Marburg. Publisher Copyright: {\textcopyright} 2015, Springer-Verlag Berlin Heidelberg.",

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doi = "10.1007/s00415-015-7921-2",

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AU - Klein, Karl Martin

AU - Pendziwiat, Manuela

AU - Cohen, Rony

AU - Appenzeller, Silke

AU - de Kovel, Carolien G.F.

AU - Rosenow, Felix

AU - Koeleman, Bobby P.C.

AU - Kuhlenbäumer, Gregor

AU - Sheintuch, Liron

AU - Veksler, Ronel

AU - Friedman, Alon

AU - Afawi, Zaid

AU - Helbig, Ingo

N1 - Funding Information: We thank the family for participation in our study. We also thank the Exome Aggregation Consortium and the groups that provided exome variant data for comparison. A full list of contributing groups can be found at http://exac.broadinstitute.org/about . The study was supported by the Deutsche Forschungsgemeinschaft with a Trilateral Grant (HE 5415/5-1) and within the EuroEPINOMICS project (HE 5415/3-1), the Christian-Albrechts-University Kiel and the Philipps-University Marburg. Publisher Copyright: © 2015, Springer-Verlag Berlin Heidelberg.

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Autosomal dominant epilepsy with auditory features: a new LGI1 family including a phenocopy with cortical dysplasia

ASJC Scopus Subject Areas

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