Associated Papers
Shared genetics in epilepsy and migraine: A scoping review.
Sahu P et al.
Epileptic Disorders : International Epilepsy Journal With Videotape, 2025
SCN1A splice variants exhibit divergent sensitivity to commonly used antiepileptic drugs.
Thompson CH et al.
Epilepsia, 2011
Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients.
Depienne C et al.
Journal of Medical Genetics, 2009
Select a paper to view details