Carnitine palmitoyltransferase type 2 deficiency: novel mutation in a Native South American family with whole-body muscle magnetic resonance imaging findings: two case reports.
J Med Case Rep
; 12(1): 249, 2018 Aug 28.
Article
in En
| MEDLINE
| ID: mdl-30149802
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Carnitine O-Palmitoyltransferase
/
Muscular Diseases
Type of study:
Diagnostic_studies
/
Observational_studies
/
Prognostic_studies
/
Risk_factors_studies
Limits:
Adolescent
/
Adult
/
Female
/
Humans
/
Male
Language:
En
Journal:
J Med Case Rep
Year:
2018
Document type:
Article
Affiliation country:
Chile
Country of publication:
Reino Unido