Review of Phenotypic Heterogeneity of Neuronal Intranuclear Inclusion Disease and
Journal
Neurology. Genetics
ISSN: 2376-7839
Titre abrégé: Neurol Genet
Pays: United States
ID NLM: 101671068
Informations de publication
Date de publication:
Apr 2024
Apr 2024
Historique:
received:
14
09
2023
accepted:
05
01
2024
medline:
8
4
2024
pubmed:
8
4
2024
entrez:
8
4
2024
Statut:
epublish
Résumé
Neuronal intranuclear inclusion disease (NIID) is an underdiagnosed neurodegenerative disorder caused by pathogenic GGC expansions in
Identifiants
pubmed: 38586597
doi: 10.1212/NXG.0000000000200132
pii: NXG-2023-000272
pmc: PMC10997217
doi:
Types de publication
Journal Article
Review
Langues
eng
Pagination
e200132Informations de copyright
Copyright © 2024 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology.
Déclaration de conflit d'intérêts
The authors report no relevant disclosures. Go to Neurology.org/NG for full disclosures.