Navigating the ALS Genetic Labyrinth: The Role of MAPT Haplotypes.
ALS
H1 haplotype
MAPT
neurodegenerative disorders
Journal
Genes
ISSN: 2073-4425
Titre abrégé: Genes (Basel)
Pays: Switzerland
ID NLM: 101551097
Informations de publication
Date de publication:
30 Oct 2023
30 Oct 2023
Historique:
received:
25
09
2023
revised:
16
10
2023
accepted:
25
10
2023
medline:
27
11
2023
pubmed:
25
11
2023
entrez:
25
11
2023
Statut:
epublish
Résumé
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by wide clinical and biological heterogeneity, with a large proportion of ALS patients also exhibiting frontotemporal dementia (FTD) spectrum symptoms. This project aimed to characterize risk subtypes of the H1 haplotype within the
Identifiants
pubmed: 38002967
pii: genes14112023
doi: 10.3390/genes14112023
pmc: PMC10671552
pii:
doi:
Substances chimiques
tau Proteins
0
MAPT protein, human
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Medical University Sofia
ID : D-186/ 14.06.2022
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