Forschung & Innovation
Publikationen
Clinical and genetic spectrum of SCN2A-associated episodic ataxia.
PMU Autor*in
Gerhard Kluger
Alle Autor*innen
N. Schwarz, T. Bast, E. Gaily, G. Golla, K M Gorman, L R Griffiths, A. Hahn, J. Hukin, M. King, C. Korff, M J Miranda, R S Møller, B. Neubauer, R A Smith, T. Smol, P. Striano, B. Stroud, M. Vaccarezza, Gerhard Kluger, H. Lerche, W. Fazeli
Fachzeitschrift
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY
Kurzfassung
Keywords
MUTATIONS, VARIANTS, SEIZURES, ENCEPHALOPATHY, NEONATAL EPILEPSY, CHANNEL GENE, SCN2A