共 50 条
- [1] 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
- [5] SCN1A Gene Mutation and Adaptive Functioning in 18 Vietnamese Children with Dravet Syndrome JOURNAL OF CLINICAL NEUROLOGY, 2017, 13 (01): : 62 - 70
- [6] A novel variant in SCN1A gene associated with Dravet syndrome SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2019, 69 : 213 - 214
- [7] Two mild cases of Dravet syndrome with truncating mutation of SCN1A BRAIN & DEVELOPMENT, 2017, 39 (01): : 72 - 74
- [8] Analysis of SCN1A mutation and parental origin in patients with Dravet syndrome Journal of Human Genetics, 2010, 55 : 421 - 427
- [10] On the likelihood of SCN1A microdeletions or duplications in Dravet syndrome with missense mutation BRAIN & DEVELOPMENT, 2012, 34 (08): : 617 - 619