A novel pathogenic mutation of MeCP2 impairs chromatin association independent of protein levels.
Genes Dev
; 37(19-20): 883-900, 2023 10 01.
Article
in En
| MEDLINE
| ID: mdl-37890975
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Chromatin
/
Rett Syndrome
Limits:
Animals
/
Female
/
Humans
/
Male
Language:
En
Journal:
Genes Dev
Journal subject:
BIOLOGIA MOLECULAR
Year:
2023
Document type:
Article
Affiliation country: