Journal
Science advances
ISSN: 2375-2548
Titre abrégé: Sci Adv
Pays: United States
ID NLM: 101653440
Informations de publication
Date de publication:
12 2023
12 2023
Historique:
medline:
1
12
2023
pubmed:
29
11
2023
entrez:
29
11
2023
Statut:
ppublish
Résumé
Copy number variations at 7q11.23 cause neurodevelopmental disorders with shared and opposite manifestations. Deletion causes Williams-Beuren syndrome featuring hypersociability, while duplication causes 7q11.23 microduplication syndrome (7Dup), frequently exhibiting autism spectrum disorder (ASD). Converging evidence indicates
Identifiants
pubmed: 38019906
doi: 10.1126/sciadv.adh2726
pmc: PMC10686562
doi:
Substances chimiques
Histone Demethylases
EC 1.14.11.-
Transcription Factors, TFIII
0
GTF2I protein, human
0
Transcription Factors, TFII
0
Gtf2i protein, mouse
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
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