Large-Scale Whole Genome Sequence Analysis of >22,000 Subjects Provides no Evidence of
ExpansionHunter
FMR1
Fragile X Syndrome
autism spectrum disorder
repeat expansion
Journal
Genes
ISSN: 2073-4425
Titre abrégé: Genes (Basel)
Pays: Switzerland
ID NLM: 101551097
Informations de publication
Date de publication:
25 07 2023
25 07 2023
Historique:
received:
26
05
2023
revised:
17
07
2023
accepted:
21
07
2023
medline:
28
8
2023
pubmed:
26
8
2023
entrez:
26
8
2023
Statut:
epublish
Résumé
Expansion of a CGG repeat in the Fragile X Messenger Ribonucleoprotein 1 (
Identifiants
pubmed: 37628570
pii: genes14081518
doi: 10.3390/genes14081518
pmc: PMC10454383
pii:
doi:
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : NIA NIH HHS
ID : RF1 AG058484
Pays : United States
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