Condition: Brugada Syndrome 5
rs104894718 in
SCN1B gene and
Brugada Syndrome 5
PMID 17020904 2007 Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutations.
PMID 5421039 1970 Arthroplasty of the temporomandibular joint.
PMID 9697698 1998 Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B.
PMID 27277800 2016 β1-C121W Is Down But Not Out: Epilepsy-Associated Scn1b-C121W Results in a Deleterious Gain-of-Function.
PMID 12011299 2002 Generalized epilepsy with febrile seizures plus: mutation of the sodium channel subunit SCN1B.
PMID 28331474 2019 Sodium Channel β Subunits in Epilepsy: Location, Location, Location.