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- [12] Two mild cases of Dravet syndrome with truncating mutation of SCN1A BRAIN & DEVELOPMENT, 2017, 39 (01): : 72 - 74
- [14] Analysis of SCN1A mutation and parental origin in patients with Dravet syndrome Journal of Human Genetics, 2010, 55 : 421 - 427
- [15] A case of Dravet Syndrome with a newly defined mutation in the SCN1A gene TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS, 2018, 53 (04): : 259 - 262
- [19] Phenotypic spectrum of the SCN1A mutation (from febrile seizures to Dravet syndrome) BRATISLAVA MEDICAL JOURNAL-BRATISLAVSKE LEKARSKE LISTY, 2022, 123 (07): : 483 - 486