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

Lookup NU author(s): Dr Rhys ThomasORCiD

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Author(s): Koko M, Motelow JE, Stanley KE, Bobbili DR, Dhindsa RS, May P, Canadian Epilepsy Network, Epi4K Consortium, Epilepsy Phenome/Genome Project, EpiPGX Consortium, EuroEPINOMICS-CoGIE Consortium

Publication type: Article

Publication status: Published

Journal: Epilepsia

Year: 2022

Volume: 63

Issue: 6

Pages: 723-735

Print publication date: 01/03/2022

Online publication date: 15/01/2022

Acceptance date: 29/12/2021

Date deposited: 06/03/2024

ISSN (electronic): 1528-1167

Publisher: Wiley

URL: https://doi.org/10.1111/epi.17166

DOI: 10.1111/epi.17166

PubMed id: 35032048

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