par Wolking, Stefan;Moreau, Claudia;McCormack, Mark;Krause, Roland;Krenn, Martin;EpiPGx Consortium, Samuel F;Berkovic, Gianpiero L;Cavalleri, Norman;Delanty, Chantal;Depondt, Michael R ;Johnson, B.P.C.;Koeleman, Wolfgang Gerhard;Kunz, Holger;Lerche, Anthony Guy;Marson, Terence;O'Brien, Slave;Petrovski, Josemir W;Sander, Graeme;Sills, Pasquale;Striano, Federico;Zara, Fritz;Zimprich, Sanjay M;Sisodiya, S;Girard, Patrick;Cossette,
Référence Annals of clinical and translational neurology, 8, 7, page (1376-1387)
Publication Publié, 2021-07-01
Référence Annals of clinical and translational neurology, 8, 7, page (1376-1387)
Publication Publié, 2021-07-01
Article révisé par les pairs
Titre: |
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Auteur: | Wolking, Stefan; Moreau, Claudia; McCormack, Mark; Krause, Roland; Krenn, Martin; EpiPGx Consortium, Samuel F; Berkovic, Gianpiero L; Cavalleri, Norman; Delanty, Chantal; Depondt, Michael R; Johnson, B.P.C.; Koeleman, Wolfgang Gerhard; Kunz, Holger; Lerche, Anthony Guy; Marson, Terence; O'Brien, Slave; Petrovski, Josemir W; Sander, Graeme; Sills, Pasquale; Striano, Federico; Zara, Fritz; Zimprich, Sanjay M; Sisodiya, S; Girard, Patrick; Cossette, |
Informations sur la publication: | Annals of clinical and translational neurology, 8, 7, page (1376-1387) |
Statut de publication: | Publié, 2021-07-01 |
Sujet CREF: | Sciences bio-médicales et agricoles |
MeSH keywords: | Cohort Studies |
Drug Resistant Epilepsy -- diagnosis -- genetics | |
Female | |
Genetic Association Studies -- methods | |
Genetic Variation -- genetics | |
Humans | |
Male | |
Polymorphism, Single Nucleotide -- genetics | |
Exome Sequencing -- methods | |
Note générale: | SCOPUS: ar.j |
Langue: | Anglais |
Identificateurs: | urn:issn:2328-9503 |
info:doi/10.1002/acn3.51374 | |
info:scp/85106975765 | |
info:pmid/34018700 | |
PMC8283173 |