Gain of Function for the SCN1A/hNav1.1-L1670W Mutation Responsible for Familial Hemiplegic Migraine

by Sandra Dhifallah, Eric Lancaster, Shana Merrill, Nathalie Leroudier, Massimo Mantegazza, Sandrine Cestèle
Published 2018-07-01

Rescuable folding defective NaV1.1 (SCN1A) mutants in epilepsy: Properties, occurrence, and novel rescuing strategy with peptides targeted to the endoplasmic reticulum

by Giulia Bechi, Raffaella Rusconi, Sandrine Cestèle, Pasquale Striano, Silvana Franceschetti, Massimo Mantegazza
Published 2015-03-01