PRRT2 MUTATIONS ARE THE MAJOR CAUSE OF BENIGN FAMILIAL INFANTILE SEIZURES (BFIS)

Capovilla, G.; Hoffmann, G.; Jurkat-Rott, K.; Antonnen, A.; Kurlemann, G.; Lehesjoki, A. E.; Lehmann-Horn, F.; Mastrangelo, M.; Mause, U.; Mueller, S.; Neubauer, B.; Puest, B.; Rating, D.; Robbiano, A.; Ruf, S.; Schroeder, C.; Seidel, A.; Specchio, N.; Stephani, U.; Striano, P.; Teichler, J.; Turkdogan, D.; Vigevano, F.; Viri, M.; Bauer, P.; Zara, F.; Lerche, H.; Weber, Y.; Schubert, J.; Paravidino, R.; Becker, F.; Berger, A.; Bebek, Nerses; Bianchi, A.; Brockmann, K.; Bernardina, B. Dalla; Fukuyama, Y.

dc.contributor.author	Capovilla, G.
dc.contributor.author	Hoffmann, G.
dc.contributor.author	Jurkat-Rott, K.
dc.contributor.author	Antonnen, A.
dc.contributor.author	Kurlemann, G.
dc.contributor.author	Lehesjoki, A. E.
dc.contributor.author	Lehmann-Horn, F.
dc.contributor.author	Mastrangelo, M.
dc.contributor.author	Mause, U.
dc.contributor.author	Mueller, S.
dc.contributor.author	Neubauer, B.
dc.contributor.author	Puest, B.
dc.contributor.author	Rating, D.
dc.contributor.author	Robbiano, A.
dc.contributor.author	Ruf, S.
dc.contributor.author	Schroeder, C.
dc.contributor.author	Seidel, A.
dc.contributor.author	Specchio, N.
dc.contributor.author	Stephani, U.
dc.contributor.author	Striano, P.
dc.contributor.author	Teichler, J.
dc.contributor.author	Turkdogan, D.
dc.contributor.author	Vigevano, F.
dc.contributor.author	Viri, M.
dc.contributor.author	Bauer, P.
dc.contributor.author	Zara, F.
dc.contributor.author	Lerche, H.
dc.contributor.author	Weber, Y.
dc.contributor.author	Schubert, J.
dc.contributor.author	Paravidino, R.
dc.contributor.author	Becker, F.
dc.contributor.author	Berger, A.
dc.contributor.author	Bebek, Nerses
dc.contributor.author	Bianchi, A.
dc.contributor.author	Brockmann, K.
dc.contributor.author	Bernardina, B. Dalla
dc.contributor.author	Fukuyama, Y.
dc.date.accessioned	2021-03-03T15:40:35Z
dc.date.available	2021-03-03T15:40:35Z
dc.identifier.citation	Weber Y., Schubert J., Paravidino R., Becker F., Berger A., Bebek N., Bianchi A., Brockmann K., Capovilla G., Bernardina B. D. , et al., "PRRT2 MUTATIONS ARE THE MAJOR CAUSE OF BENIGN FAMILIAL INFANTILE SEIZURES (BFIS)", 10th European Congress on Epileptology, London, Kanada, 30 Eylül - 04 Ekim 2012, cilt.53, ss.2
dc.identifier.other	vv_1032021
dc.identifier.other	av_4031b125-4e34-4a06-8eb8-5e0c0b6ecf88
dc.identifier.uri	http://hdl.handle.net/20.500.12627/46928
dc.identifier.uri	https://doi.org/10.1111/j.1528-1167.2012.03679.x
dc.language.iso	eng
dc.subject	Neurology
dc.subject	Health Sciences
dc.subject	Nöroloji
dc.subject	Neurology (clinical)
dc.subject	Life Sciences
dc.subject	Sağlık Bilimleri
dc.subject	KLİNİK NEUROLOJİ
dc.subject	Klinik Tıp
dc.subject	Klinik Tıp (MED)
dc.subject	Tıp
dc.subject	Dahili Tıp Bilimleri
dc.title	PRRT2 MUTATIONS ARE THE MAJOR CAUSE OF BENIGN FAMILIAL INFANTILE SEIZURES (BFIS)
dc.type	Bildiri
dc.contributor.department	Eberhard Karls University of Tubingen , ,
dc.identifier.volume	53
dc.contributor.firstauthorID	2482865

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