Oligogenicity, C9orf72 expansion, and variant severity in ALS.
ALS
C9orf72 expansion
Oligogenicity
Variant severity
Journal
Neurogenetics
ISSN: 1364-6753
Titre abrégé: Neurogenetics
Pays: United States
ID NLM: 9709714
Informations de publication
Date de publication:
07 2020
07 2020
Historique:
received:
17
01
2020
accepted:
04
04
2020
pubmed:
10
5
2020
medline:
16
6
2021
entrez:
10
5
2020
Statut:
ppublish
Résumé
"Oligogenic inheritance" is used to describe cases where more than one rare pathogenic variant is observed in the same individual. While multiple variants can alter disease presentation, the necessity of multiple variants to instigate pathogenesis has not been addressed in amyotrophic lateral sclerosis (ALS). We sequenced ALS-associated genes in C9orf72-expansion-positive and negative ALS patients, alongside unaffected controls, to test the importance of oligogenicity and variant deleteriousness in ALS. We found that all groups had similar numbers of rare variants, but that variant severity was significantly higher in C9orf72-negative ALS cases, suggesting sufficiency of C9orf72 expansion to cause ALS alone.
Identifiants
pubmed: 32385536
doi: 10.1007/s10048-020-00612-7
pii: 10.1007/s10048-020-00612-7
doi:
Substances chimiques
C9orf72 Protein
0
C9orf72 protein, human
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
227-242Subventions
Organisme : CIHR
ID : FRN 159279
Pays : Canada