Altered Bone Status in Rett Syndrome.
MeCP2
WNT pathway
bone metabolism
bone mineral density
osteoblast
Journal
Life (Basel, Switzerland)
ISSN: 2075-1729
Titre abrégé: Life (Basel)
Pays: Switzerland
ID NLM: 101580444
Informations de publication
Date de publication:
03 Jun 2021
03 Jun 2021
Historique:
received:
10
05
2021
revised:
31
05
2021
accepted:
02
06
2021
entrez:
2
7
2021
pubmed:
3
7
2021
medline:
3
7
2021
Statut:
epublish
Résumé
Rett syndrome (RTT) is a monogenic neurodevelopmental disorder primarily caused by mutations in X-linked
Identifiants
pubmed: 34205017
pii: life11060521
doi: 10.3390/life11060521
pmc: PMC8230033
pii:
doi:
Types de publication
Journal Article
Review
Langues
eng
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