Supplements to the article: Association of ultra-rare coding variants with genetic generalized epilepsy: a case-control whole exome sequencing study

Name: Supplements to the article: Association of ultra-rare coding variants with genetic generalized epilepsy: a case-control whole exome sequencing study
Creator: Mahmoud Koko
Published: 2021-12-30T14:37:31.341Z
Keywords: Genetic Generalized Epilepsy

Koko, Mahmoud; Motelow, Joshua; Stanley, Kate; Bobbili, Dheeraj; Dhindsa, Ryan; May, Patrick; Consortia, CENet, Epi4K, EP/GP, Epicure, EpiPGX and EuroEPINOMICS-CoGIE

doi:10.17632/5p556jtwt9.1

Supplements to the article: Association of ultra-rare coding variants with genetic generalized epilepsy: a case-control whole exome sequencing study

Published: 30 December 2021| Version 1 | DOI: 10.17632/5p556jtwt9.1

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,

, CENet, Epi4K, EP/GP, Epicure, EpiPGX and EuroEPINOMICS-CoGIE Consortia

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Supplemental data to the article "Association of ultra-rare coding variants with genetic generalized epilepsy: a case-control whole exome sequencing study".

Supplements to the article: Association of ultra-rare coding variants with genetic generalized epilepsy: a case-control whole exome sequencing study

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