A novel SCN1A mutation associated with severe GEFS+ in a large South American pedigree

Proposal for Revised Classification of Epilepsies and Epileptic Syndromes

Epilepsia · 1989 · 5.4K citations

Medicine, Neurology, Neuroscience +12

Strategies for multilocus linkage analysis in humans.

G.M. Lathrop, J.-M. Lalouel, Cécile Julier et al. · Proceedings of the National Academy of Sciences · 1984 · 2.6K citations · Full text

Life Sciences, Genetics, Genomics +16

Experience with the International League Against Epilepsy Proposals for Classification of Epileptic Seizures and the Epilepsies and Epileptic Syndromes in a Pediatric Outpatient Epilepsy Clinic

Jorge Eslava‐Cobos, Daniel Naririo · Epilepsia · 1989 · 1.3K citations

Medicine, Neurology, Pediatrics +16

De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy

Lieve Claes, Jurgen Del‐Favero, Berten Ceulemans et al. · The American Journal of Human Genetics · 2001 · 1.3K citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B

Robyn H. Wallace, Dao Wen Wang, Rita Singh et al. · Nature Genetics · 1998 · 1K citations

Life Sciences, Genetics, Neuroscience +14