Your browser doesn't support javascript.
loading
Evaluation of a mitochondrial DNA mutation in maternally inherited and sporadic cases of Dupuytren disease.
Anderson, Eric R; Burmester, James K; Caldwell, Michael D.
Affiliation
  • Anderson ER; Department of General Surgery, Marshfield Clinic, Wisconsin 54449, USA. anderson.eric@marshfieldclinic.org
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

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