Consulter en ligne

Suggestions

Du même auteur

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

Archive ouverte | Cestèle, Sandrine | CCSD

International audience

Loss-of-function KCNH2 mutation in a family with long QT syndrome, epilepsy, and sudden death

Archive ouverte | Cestèle, Sandrine | CCSD

International audience

Divergent effects of the T1174S SCN1A mutation associated with seizures and hemiplegic migraine

Archive ouverte | Cestèle, Sandrine | CCSD

International audience

Chargement des enrichissements...