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Understanding Epilepsy Genetics

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Tag Archives: KCNC3

Five unexpected things I realized at AES this year

Posted on December 9, 2014 by Ingo Helbig (Kiel)

Seattle 2014. This year, the 68th Annual Meeting of the American Epilepsy Society was held in Seattle. While much of the scientific content of AES is still under publication embargo and will be the topic of our next post, here are five unexpected things I learned at AES this year. Continue reading →

Posted in 2014, Opinion
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autism autosomal recessive disorders CACNA1A CDKL5 CHD2 CNV de novo mutations DEPDC5 DNM1 Dravet Syndrome Epi4K epilepsy epilepsy gene epilepsy genetics epileptic encephalopathy EuroEPINOMICS exome exome sequencing febrile seizures GABRA1 GABRG2 GEFS+ genetic architecture genome sequencing GRIN2A GWAS Idiopathic Generalized Epilepsy IGE Infantile Spasms intellectual disability juvenile myoclonic epilepsy KCNQ2 KCNT1 microdeletion precision medicine rare variants science SCN1A SCN1B SCN2A SCN8A STXBP1 SYNGAP1 whole exome sequencing whole genome sequencing

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