Association of ultra-rare coding variants with genetic generalized epilepsy: A case–control whole exome sequencing study

Canadian Epilepsy Network, Epi4K Consortium, Epilepsy Phenome/Genome Project, EpiPGX Consortium, EuroEPINOMICS-CoGIE Consortium

Research output: Contribution to journalArticlepeer-review

Fingerprint

Dive into the research topics of 'Association of ultra-rare coding variants with genetic generalized epilepsy: A case–control whole exome sequencing study'. Together they form a unique fingerprint.

Medicine & Life Sciences