Hammer MF, Pan Y, Cumbay M, Pendziwiat M, et al. Whole exome sequencing and co-expression analysis identify an SCN1A variant that modifies pathogenicity in a family with Genetic Epilepsy and Febrile Seizures Plus (GEFS+). Epilepsia 2022 May 20. doi: 10.1111/epi.17296.
PMID: 35592948