A novel compound heterozygous mutation in PYGM gene associated with McArdle's disease.
Acta Myol
; 41(1): 37-40, 2022 Mar.
Article
in En
| MEDLINE
| ID: mdl-35465342
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Glycogen Storage Disease Type V
/
Glycogen Phosphorylase, Muscle Form
Type of study:
Diagnostic_studies
/
Risk_factors_studies
Limits:
Adolescent
/
Humans
/
Male
Language:
En
Journal:
Acta Myol
Journal subject:
CARDIOLOGIA
/
FISIOLOGIA
Year:
2022
Document type:
Article
Affiliation country:
Country of publication: