CHAMP1
MRD40
intellectual disability
metabolic syndrome
neurodevelopmental delay
Journal
Genes
ISSN: 2073-4425
Titre abrégé: Genes (Basel)
Pays: Switzerland
ID NLM: 101551097
Informations de publication
Date de publication:
28 07 2023
28 07 2023
Historique:
received:
24
06
2023
revised:
26
07
2023
accepted:
27
07
2023
medline:
28
8
2023
pubmed:
26
8
2023
entrez:
26
8
2023
Statut:
epublish
Résumé
Intellectual disability (ID) is a prevalent neurodevelopmental disorder characterized by limitations in intellectual functioning and adaptive behavior. While the causes of ID are still largely unknown, it is believed to result from a combination of environmental exposures and genetic abnormalities. Recent advancements in genomic studies and clinical genetic testing have identified numerous genes associated with neurodevelopmental disorders (NDDs), including ID. One such gene is
Identifiants
pubmed: 37628598
pii: genes14081546
doi: 10.3390/genes14081546
pmc: PMC10454041
pii:
doi:
Substances chimiques
CHAMP1 protein, human
0
Chromosomal Proteins, Non-Histone
0
Phosphoproteins
0
Types de publication
Review
Case Reports
Langues
eng
Sous-ensembles de citation
IM
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