Distinct gene-set burden patterns underlie common generalized and focal epilepsies
- Resource Type
- Source
- EBioMedicine
EBioMedicine 72, 103588 (2021). doi:10.1016/j.ebiom.2021.103588
eBioMedicine, Amsterdam : Elsevier BV, 2021, vol. 72, art. no. 103588, p. [1-13]
EBioMedicine, Vol 72, Iss, Pp 103588-(2021) - Subject
Exome sequencing Male Medicine (General) Neurology [D14] [Human health sciences] Gene-set Genome-wide association study Disease Biology Epileptogenesis General Biochemistry, Genetics and Molecular Biology Whole Exome Sequencing Epilepsy R5-920 medicine Missense mutation Humans Exome Genetic Predisposition to Disease Gene Genetic association Ultra-rare variant Genetics Neurologie [D14] [Sciences de la santé humaine] Burden analysis Genetic Variation General Medicine medicine.disease Ultra-rare variants Gene-sets Case-Control Studies Medicine epilepsy Epilepsy, Generalized Female Genetics & genetic processes [F10] [Life sciences] Epilepsies, Partial Human medicine Burden analysi Génétique & processus génétiques [F10] [Sciences du vivant] Case-Control Studie Research Paper Genome-Wide Association Study Human - Language
- English
- ISSN
- 2352-3964