Mice lacking MBNL1 and MBNL2 exhibit sudden cardiac death and molecular signatures recapitulating myotonic dystrophy.
Hum Mol Genet
; 31(18): 3144-3160, 2022 09 10.
Article
in En
| MEDLINE
| ID: mdl-35567413
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Myotonic Dystrophy
Type of study:
Etiology_studies
Limits:
Animals
Language:
En
Journal:
Hum Mol Genet
Journal subject:
BIOLOGIA MOLECULAR
/
GENETICA MEDICA
Year:
2022
Type:
Article
Affiliation country:
Taiwan