Skeletal muscle cell protein dysregulation highlights the pathogenesis mechanism of myopathy-associated p97/VCP R155H mutations.
Front Neurol
; 14: 1211635, 2023.
Article
in En
| MEDLINE
| ID: mdl-37602234
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Type of study:
Etiology_studies
/
Prognostic_studies
/
Risk_factors_studies
Language:
En
Journal:
Front Neurol
Year:
2023
Document type:
Article
Affiliation country:
United States
Country of publication:
Switzerland