Condition: GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1
rs104894718
in
SCN1B
gene and
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1
PMID 21040232
2011 New mutation c.374C>T and a putative disease-associated haplotype within SCN1B gene in Tunisian families with febrile seizures.
PMID 17928445
2007 Modulatory proteins can rescue a trafficking defective epileptogenic Nav1.1 Na+ channel mutant.
PMID 9697698
1998 Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B.