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Understanding Epilepsy Genetics

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Tag Archives: Epilepsy Blog Relay

Epilepsy Blog Relay 2015: Five things to know about epilepsy and genes

Posted on November 10, 2015 by Ingo Helbig

Epilepsy Awareness Month. Today, we have contributed a guest post to this November’s Epilepsy Blog Relay on livingwellwithepilepsy.com. Here are the five things about epilepsy and genes that may be interesting for people with epilepsy to know. Click here.
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Posted in Guidance, Opinion
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autism autosomal recessive disorders CACNA1A CDKL5 CHD2 CNV de novo mutations DEPDC5 DNM1 Dravet Syndrome Epi4K epilepsy epilepsy genetics epileptic encephalopathy EuroEPINOMICS exome exome sequencing febrile seizures GABRA1 GABRG2 GEFS+ genetic architecture genome sequencing GGE 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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