TY - JOUR
T1 - Progressive myoclonus epilepsy caused by a gain-of-function KCNA2 mutation
AU - Canafoglia, Laura
AU - Castellotti, Barbara
AU - Ragona, Francesca
AU - Freri, Elena
AU - Granata, Tiziana
AU - Chiapparini, Luisa
AU - Gellera, Cinzia
AU - Scaioli, Vidmer
AU - Franceschetti, Silvana
AU - DiFrancesco, Jacopo C.
PY - 2019/2/1
Y1 - 2019/2/1
KW - Genetic ataxia
KW - KCNA2 gene
KW - Potassium channelopathy
KW - Progressive myoclonus epilepsy
UR - http://www.scopus.com/inward/record.url?scp=85060095623&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85060095623&partnerID=8YFLogxK
U2 - 10.1016/j.seizure.2019.01.005
DO - 10.1016/j.seizure.2019.01.005
M3 - Article
AN - SCOPUS:85060095623
VL - 65
SP - 106
EP - 108
JO - Seizure : the journal of the British Epilepsy Association
JF - Seizure : the journal of the British Epilepsy Association
SN - 1059-1311
ER -