ASFMR1/FMR4 gene
FMR1 gene
fragile X syndrome
large deletion
miRNA
Journal
Frontiers in genetics
ISSN: 1664-8021
Titre abrégé: Front Genet
Pays: Switzerland
ID NLM: 101560621
Informations de publication
Date de publication:
2022
2022
Historique:
received:
26
02
2022
accepted:
13
04
2022
entrez:
1
6
2022
pubmed:
2
6
2022
medline:
2
6
2022
Statut:
epublish
Résumé
Fragile X syndrome (FXS) is the most frequent cause of X-linked inherited intellectual disabilities (ID) and the most frequent monogenic form of autism spectrum disorders. It is caused by an expansion of a CGG trinucleotide repeat located in the 5'UTR of the
Identifiants
pubmed: 35646065
doi: 10.3389/fgene.2022.884424
pii: 884424
pmc: PMC9130735
doi:
Types de publication
Journal Article
Langues
eng
Pagination
884424Informations de copyright
Copyright © 2022 Jiraanont, Manor, Tabatadze, Zafarullah, Mendoza, Melikishvili and Tassone.
Déclaration de conflit d'intérêts
FT received funds from Azrieli Foundation and Zynerba for studies on Fragile X syndrome. The remaining authors declared that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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