The role of rare genetic variants enrichment in epilepsies of presumed genetic etiology.
Journal
medRxiv : the preprint server for health sciences
Titre abrégé: medRxiv
Pays: United States
ID NLM: 101767986
Informations de publication
Date de publication:
10 Mar 2023
10 Mar 2023
Historique:
medline:
29
3
2023
entrez:
28
3
2023
pubmed:
29
3
2023
Statut:
epublish
Résumé
Previous studies suggested that severe epilepsies e.g., developmental and epileptic encephalopathies (DEE) are mainly caused by ultra-rare
Identifiants
pubmed: 36974069
doi: 10.1101/2023.01.17.23284702
pmc: PMC10041669
pii:
doi:
Types de publication
Preprint
Langues
eng
Subventions
Organisme : NHGRI NIH HHS
ID : U01 HG009088
Pays : United States
Organisme : NHGRI NIH HHS
ID : UM1 HG008895
Pays : United States
Commentaires et corrections
Type : UpdateIn
Déclaration de conflit d'intérêts
11.Conflict of Interest The authors declare no competing interests.
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