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scn1a
- The SCN1A gene belongs to a family of genes that provide instructions for making sodium channels. These channels, which transport positively charged sodium ...
- ... cause GEFS+. The most commonly associated gene is SCN1A. More than 80 percent of Dravet syndrome cases ... small number of affected individuals or families.The SCN1A gene and others associated with GEFS+ provide instructions ...
- ... often than males. Mutations in the CACNA1A, ATP1A2, SCN1A, and PRRT2 genes have been found to cause ... believe that mutations in the CACNA1A, ATP1A2, and SCN1A genes can upset the balance of ions in ...
- ... when coupled with variants in another gene called SCN1A, alter the progression of a seizure disorder called ... alertness that can last from hours to weeks. SCN1A gene variants are the most common cause of ...
- Epilepsy/Specifics ... Epilepsy ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health ... Dravet syndrome is an epilepsy ...
- ... disorder, such as tuberous sclerosis complex. CHD2 FOXG1 SCN1A SCN8A STXBP1 Additional Information from NCBI Gene: ALG13 ... Lund C, Brandal K, Undlien DE, Brodtkorb E. SCN1A mutation screening in adult patients with Lennox-Gastaut ...
- Curing the Epilepsies: The Promise of Research
(National Institute of Neurological Disorders and Stroke)
Epilepsy/Statistics and Research ... Epilepsy ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health ... Curing the Epilepsies: ... - ... delay that is characteristic of this condition. KCNT1 SCN1A TBC1D24 MMPSI is not inherited from a parent ...