Most common NOTCH3 mutations causing CADASIL or CADASIL-like cerebral small vessel disease: A systematic review.
CADASIL
Dementia
Mutation
NOTCH3
Phenotype
Journal
Cerebral circulation - cognition and behavior
ISSN: 2666-2450
Titre abrégé: Cereb Circ Cogn Behav
Pays: Netherlands
ID NLM: 101774849
Informations de publication
Date de publication:
2024
2024
Historique:
received:
01
01
2024
revised:
09
05
2024
accepted:
30
05
2024
medline:
5
7
2024
pubmed:
5
7
2024
entrez:
5
7
2024
Statut:
epublish
Résumé
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) is a monogenic disorder caused by mutations in the
Identifiants
pubmed: 38966425
doi: 10.1016/j.cccb.2024.100227
pii: S2666-2450(24)00028-X
pmc: PMC11223087
doi:
Types de publication
Journal Article
Review
Langues
eng
Pagination
100227Informations de copyright
© 2024 The Authors. Published by Elsevier B.V.
Déclaration de conflit d'intérêts
The authors declare no competing financial interests.