Somatosensory reflex seizures in a child with epilepsy related to novel SCN1A mutation

[1] Lossin C(2009)A catalog of SCN1A variants Brain and Development 31 114-130

[2] Meng H(2015)The SCN1A mutation database: updating information and analysis of the relationships among genotype, functional alteration, and phenotype Hum Mutat 36 573-580

[3] Xu HQ(2013)SCN1A testing for epilepsy: application in clinical practice Epilepsia 54 946-952

[4] Yu L(2013)The pharmacologic treatment of Dravet syndrome Epilepsia 52 72-75

[5] Lin GW(2010)Variable epilepsy phenotypes associated with a familial intragenic deletion of the SCN1A gene Epilepsia 51 2474e7-410

[6] He N(2010)Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndrome J Med Genet 47 404-1332

[7] Su T(2011)De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy Am J Hum Genet 68 1327-29

[8] Hirose S(2011)The genetics of Dravet syndrome Epilepsia 52 24-12

[9] Scheffer IE(2011)Borderline Dravet syndrome: a useful diagnostic category? Epilepsia 52 10-212

[10] Marini C(2011)Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutations Epilepsia 52 1251e7-1888

[1] Lossin C(2009)A catalog of SCN1A variants Brain and Development 31 114-130

[2] Meng H(2015)The SCN1A mutation database: updating information and analysis of the relationships among genotype, functional alteration, and phenotype Hum Mutat 36 573-580

[3] Xu HQ(2013)SCN1A testing for epilepsy: application in clinical practice Epilepsia 54 946-952

[4] Yu L(2013)The pharmacologic treatment of Dravet syndrome Epilepsia 52 72-75

[5] Lin GW(2010)Variable epilepsy phenotypes associated with a familial intragenic deletion of the SCN1A gene Epilepsia 51 2474e7-410

[6] He N(2010)Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndrome J Med Genet 47 404-1332

[7] Su T(2011)De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy Am J Hum Genet 68 1327-29

[8] Hirose S(2011)The genetics of Dravet syndrome Epilepsia 52 24-12

[9] Scheffer IE(2011)Borderline Dravet syndrome: a useful diagnostic category? Epilepsia 52 10-212

[10] Marini C(2011)Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutations Epilepsia 52 1251e7-1888