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

Klein, K. M.; Pendziwiat, M.; Cohen, R.; Appenzeller, S.; De Kovel, Carolien G. F.; Rosenow, F.; Koeleman, B. P.; Kuhlenbaumer, G.; Sheintuch, L.; Veksler, R.; Friedman, A.; Afawi, Z.; Helbig, I.

doi:10.1007/s00415-015-7921-2

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

Klein, K. M., Pendziwiat, M., Cohen, R., Appenzeller, S., De Kovel, C. G. F., Rosenow, F., et al. (2016). Autosomal dominant epilepsy with auditory features: a new LGI1 family including a phenocopy with cortical dysplasia. Journal of Neurology, 263(1), 11-6. doi:10.1007/s00415-015-7921-2.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-002B-9C58-1 Version Permalink: https://hdl.handle.net/11858/00-001M-0000-002B-9C59-0

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Creators:
Klein, K. M., Author
Pendziwiat, M., Author
Cohen, R., Author
Appenzeller, S., Author
De Kovel, Carolien G. F.¹, Author
Rosenow, F., Author
Koeleman, B. P., Author
Kuhlenbaumer, G., Author
Sheintuch, L., Author
Veksler, R., Author
Friedman, A., Author
Afawi, Z., Author
Helbig, I., Author

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1University Medical Center Utrecht, ou_persistent22

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Language(s): eng - English

Dates: Date issued: 2016

Publication Status: Issued

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Rev. Type: Peer

Identifiers: DOI: 10.1007/s00415-015-7921-2

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Title: Journal of Neurology

Source Genre: Journal

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Publ. Info: Berlin [etc.] : Springer

Pages: - Volume / Issue: 263 (1) Sequence Number: - Start / End Page: 11 - 6 Identifier: ISSN: 0340-5354
CoNE: https://pure.mpg.de/cone/journals/resource/110978979590419