Identification of FHL1 as a therapeutic target for Duchenne muscular dystrophy.
Hum Mol Genet
; 23(3): 618-36, 2014 Feb 01.
Article
in En
| MEDLINE
| ID: mdl-24087791
Full text:
1
Database:
MEDLINE
Main subject:
Muscular Dystrophy, Duchenne
/
Intracellular Signaling Peptides and Proteins
/
LIM Domain Proteins
/
Muscle Proteins
Type of study:
Diagnostic_studies
/
Prognostic_studies
Limits:
Animals
/
Humans
Language:
En
Journal:
Hum Mol Genet
Journal subject:
BIOLOGIA MOLECULAR
/
GENETICA MEDICA
Year:
2014
Type:
Article
Affiliation country:
Australia