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Association of SLC32A1 Missense Variants With Genetic Epilepsy With Febrile Seizures Plus
UploadBRAT1-associated neurodegeneration: Intra-familial phenotypic differences in siblings
Download from api.wiley.comMultiplex families with epilepsy
Download from www.ncbi.nlm.nih.govBenign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation
Download from dx.doi.orgFamilial neonatal seizures in 36 families: Clinical and genetic features correlate with outcome
Download from www.researchgate.netMutations in KCNT1 cause a spectrum of focal epilepsies
UploadA recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy
Download from www.nature.comKCNT1 Gain of Function in 2 Epilepsy Phenotypes is Reversed by Quinidine
Download from www.ncbi.nlm.nih.govAutosomal dominant vasovagal syncope
UploadMutations in DEPDC5 cause familial focal epilepsy with variable foci
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