Unraveling Molecular Pathways Altered in MeCP2-Related Syndromes, in the Search for New Potential Avenues for Therapy.
MECP2 duplication syndrome
MeCP2
Rett syndrome
miRNA biomarkers
microcephaly
Journal
Biomedicines
ISSN: 2227-9059
Titre abrégé: Biomedicines
Pays: Switzerland
ID NLM: 101691304
Informations de publication
Date de publication:
03 Feb 2021
03 Feb 2021
Historique:
received:
22
12
2020
revised:
25
01
2021
accepted:
30
01
2021
entrez:
6
2
2021
pubmed:
7
2
2021
medline:
7
2
2021
Statut:
epublish
Résumé
Methyl-CpG-binding protein 2 (MeCP2) is an X-linked epigenetic modulator whose dosage is critical for neural development and function. Loss-of-function mutations in
Identifiants
pubmed: 33546327
pii: biomedicines9020148
doi: 10.3390/biomedicines9020148
pmc: PMC7913493
pii:
doi:
Types de publication
Journal Article
Langues
eng
Subventions
Organisme : Instituto de Salud Carlos III
ID : PI15/01082
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