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Koko, Mahmoud ORCID: 0000-0001-9512-0184, Motelow, Joshua E ORCID: 0000-0002-4367-4182, Stanley, Kate E ORCID: 0000-0002-2861-9660, Bobbili, Dheeraj R ORCID: 0000-0002-1368-9623, Dhindsa, Ryan S ORCID: 0000-0002-8965-0813, May, Patrick ORCID: 0000-0001-8698-3770, Canadian Epilepsy Network, , Epi4K Consortium, , Epilepsy Phenome/Genome Project, , EpiPGX Consortium,
et al (show 1 more authors) (2022) Association of ultra-rare coding variants with genetic generalized epilepsy: A case-control whole exome sequencing study. Epilepsia, 63 (3). 723 - 735.


Epi4K consortium, and Epilepsy Phenome/Genome Project,
(2017) Ultra-rare genetic variation in common epilepsies: a case-control sequencing study. The Lancet. Neurology, 16 (2). 135 - 143.

This list was generated on Sun Jul 31 12:41:04 2022 BST.