Association of
Journal
Neurology
ISSN: 1526-632X
Titre abrégé: Neurology
Pays: United States
ID NLM: 0401060
Informations de publication
Date de publication:
04 05 2021
04 05 2021
Historique:
received:
08
09
2020
accepted:
05
02
2021
entrez:
26
5
2021
pubmed:
27
5
2021
medline:
9
6
2021
Statut:
ppublish
Résumé
To identify the causative gene in a large unsolved family with genetic epilepsy with febrile seizures plus (GEFS+), we sequenced the genomes of family members, and then determined the contribution of the identified gene to the pathogenicity of epilepsies by examining sequencing data from 2,772 additional patients. We performed whole genome sequencing of 3 members of a GEFS+ family. Subsequently, whole exome sequencing data from 1,165 patients with epilepsy from the Epi4K dataset and 1,329 Australian patients with epilepsy from the Epi25 dataset were interrogated. Targeted resequencing was performed on 278 patients with febrile seizures or GEFS+ phenotypes. Variants were validated and familial segregation examined by Sanger sequencing. Eight previously unreported missense variants were identified in Missense variants in
Identifiants
pubmed: 34038384
pii: WNL.0000000000011855
doi: 10.1212/WNL.0000000000011855
pmc: PMC8166436
doi:
Substances chimiques
SLC32A1 protein, human
0
Vesicular Inhibitory Amino Acid Transport Proteins
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e2251-e2260Commentaires et corrections
Type : CommentIn
Informations de copyright
© 2021 American Academy of Neurology.
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