权威例句
Severe myoclonic epilepsy in infancy: Dravet syndrome
Juvenile Myoclonic Epilepsy: A 5-Year Prospective Study
Severe myoclonic epilepsy of infancy: extended spectrum of GEFS+?
Mutations in EFHC1 cause juvenile myoclonic epilepsy
Lamotrigine and seizure aggravation in severe myoclonic epilepsy
Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation.
Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy.
De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy.
Shoffner, J. M. et al. Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNALYS mutati...
Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy