Evaluation of a mitochondrial DNA mutation in maternally inherited and sporadic cases of dupuytren disease

Clinical Medicine and Research

Volumn 10, Issue 3, 2012, Pages 122-126

  Anderson, Eric R ^a   Burmester, James K ^a   Caldwell, Michael D ^a  

^a MARSHFIELD CLINIC   (United States)

Author keywords

Dupuytren disease; Mitochondrial DNA; Mutation

Indexed keywords

MITOCHONDRIAL DNA;

ALLELE; ARTICLE; CONTROLLED STUDY; DNA SEQUENCE; DUPUYTREN CONTRACTURE; ELECTRONIC MEDICAL RECORD; EXTRACHROMOSOMAL INHERITANCE; FAMILY HISTORY; FEMALE; GENE MUTATION; GENETIC ANALYSIS; GENETIC POLYMORPHISM; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; PATHOGENESIS;

CASE-CONTROL STUDIES; DNA, MITOCHONDRIAL; DUPUYTREN CONTRACTURE; FEMALE; GENETIC DISEASES, INBORN; HUMANS; MALE; POINT MUTATION; POLYMORPHISM, GENETIC;

EID: 84865322890     PISSN: 15394182     EISSN: 15546179     Source Type: Journal    
DOI: 10.3121/cmr.2012.1063     Document Type: Article

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