ATP13A2 (PARK9) and basal ganglia function.
Kufor-Rakeb Syndrome
Parkinson’s disease
alpha-synuclein
iron
manganese
mitochondria
neuronal ceroid lipofuscinosis
zinc
Journal
Frontiers in neurology
ISSN: 1664-2295
Titre abrégé: Front Neurol
Pays: Switzerland
ID NLM: 101546899
Informations de publication
Date de publication:
2023
2023
Historique:
received:
05
07
2023
accepted:
11
12
2023
medline:
22
1
2024
pubmed:
22
1
2024
entrez:
22
1
2024
Statut:
epublish
Résumé
ATP13A2 is a lysosomal protein involved in polyamine transport with loss of function mutations associated with multiple neurodegenerative conditions. These include early onset Parkinson's disease, Kufor-Rakeb Syndrome, neuronal ceroid lipofuscinosis, hereditary spastic paraplegia, and amyotrophic lateral sclerosis. While
Identifiants
pubmed: 38249738
doi: 10.3389/fneur.2023.1252400
pmc: PMC10796451
doi:
Types de publication
Journal Article
Review
Langues
eng
Pagination
1252400Informations de copyright
Copyright © 2024 Croucher and Fleming.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.