Molecular Biomarkers in Fragile X Syndrome.
ASD.
FMR1
FMRP
Fmr1 KO mouse
fragile X syndrome
intellectual disability
molecular biomarkers
Journal
Brain sciences
ISSN: 2076-3425
Titre abrégé: Brain Sci
Pays: Switzerland
ID NLM: 101598646
Informations de publication
Date de publication:
27 Apr 2019
27 Apr 2019
Historique:
received:
07
03
2019
revised:
22
04
2019
accepted:
24
04
2019
entrez:
1
5
2019
pubmed:
1
5
2019
medline:
1
5
2019
Statut:
epublish
Résumé
Fragile X syndrome (FXS) is the most common inherited form of intellectual disability (ID) and a known monogenic cause of autism spectrum disorder (ASD). It is a trinucleotide repeat disorder, in which more than 200 CGG repeats in the 5' untranslated region (UTR) of the fragile X mental retardation 1 (
Identifiants
pubmed: 31035599
pii: brainsci9050096
doi: 10.3390/brainsci9050096
pmc: PMC6562871
pii:
doi:
Types de publication
Journal Article
Review
Langues
eng
Subventions
Organisme : NIGMS NIH HHS
ID : R01 GM113929
Pays : United States
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