Associated Papers
Genotype-phenotype associations in 1018 individuals with SCN1A-related epilepsies.
Gallagher D et al.
Epilepsia, 2024
Modifier genes in SCN1A-related epilepsy syndromes.
de Lange IM et al.
Molecular Genetics & Genomic Medicine, 2020
32032478 (PubMed )
Supplement: MGG3-8-e1103-s006.pdf
Select a paper to view details