Evaluation of a mitochondrial DNA mutation in maternally inherited and sporadic cases of Dupuytren disease.
Clin Med Res
; 10(3): 122-6, 2012 Aug.
Article
in En
| MEDLINE
| ID: mdl-22634541
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Polymorphism, Genetic
/
DNA, Mitochondrial
/
Point Mutation
/
Dupuytren Contracture
/
Genetic Diseases, Inborn
Type of study:
Observational_studies
/
Prognostic_studies
/
Risk_factors_studies
Limits:
Female
/
Humans
/
Male
Language:
En
Journal:
Clin Med Res
Year:
2012
Document type:
Article
Affiliation country:
United States
Country of publication:
United States