Expression of FMRpolyG in Peripheral Blood Mononuclear Cells of Women with Fragile X Mental Retardation 1 Gene Premutation.
FMR1 premutation
FMRpolyG
premature ovarian insufficiency
Journal
Genes
ISSN: 2073-4425
Titre abrégé: Genes (Basel)
Pays: Switzerland
ID NLM: 101551097
Informations de publication
Date de publication:
01 03 2022
01 03 2022
Historique:
received:
10
02
2022
revised:
24
02
2022
accepted:
28
02
2022
entrez:
25
3
2022
pubmed:
26
3
2022
medline:
28
4
2022
Statut:
epublish
Résumé
Fragile X-associated primary ovarian insufficiency (FXPOI) is characterized by oligo/amenorrhea and hypergonadotropic hypogonadism and is caused by the expansion of the CGG repeat in the 5'UTR of Fragile X Mental Retardation 1 (
Identifiants
pubmed: 35328005
pii: genes13030451
doi: 10.3390/genes13030451
pmc: PMC8951797
pii:
doi:
Substances chimiques
FMR1 protein, human
0
Fragile X Mental Retardation Protein
139135-51-6
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
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