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Genotype-phenotype Associations in 1018 Individuals with SCN1A-related Epilepsies

Declan Gallagher,Eduardo Perez-Palma,Tobias Bruenger,Ismael Ghanty,Eva Brilstra,Berten Ceulemans,Nicole Chemaly,Iris de Lange,Christel Depienne,Renzo Guerrini,Davide Mei,Rikke S. Moller,Rima Nabbout,Brigid M. Regan,Amy L. Schneider,Ingrid E. Scheffer,An-Sofie Schoonjans,Joseph D. Symonds,Sarah Weckhuysen,Sameer M. Zuberi,Dennis Lal,Andreas Brunklaus

EPILEPSIA（2024）

Cited 3|Views49
Key words
Dravet syndrome,GEFS plus,genotype-phenotype associations,SCN1A,severe myoclonic epilepsy of infancy
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