The mitochondrial T16189C polymorphism is associated with coronary artery disease in Middle European populations

PLoS ONE

Volumn 6, Issue 1, 2011, Pages

  Mueller, Edith E ^a   Eder, Waltraud ^a   Ebner, Sabine ^a   Schwaiger, Eva ^a   Santic, Danijela ^a   Kreindl, Tanja ^a   Stanger, Olaf ^a   Paulweber, Bernhard ^a   Iglseder, Bernhard ^a   Oberkofler, Hannes ^a   Maier, Richard ^b   Mayr, Johannes A ^a   Krempler, Franz ^c   Weitgasser, Raimund ^a   Patsch, Wolfgang ^a   Sperl, Wolfgang ^a   Kofler, Barbara ^a  

^a PARACELSUS MEDICAL UNIVERSITY   (Austria)

^b MEDICAL UNIVERSITY OF GRAZ   (Austria)

^c Hospital Hallein   (Austria)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ADULT; AGE; AGED; ARTICLE; AUSTRIA; CONTROLLED STUDY; CORONARY ARTERY DISEASE; DNA SEQUENCE; ETHNICITY; EUROPE; FEMALE; GENDER; GENE MUTATION; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC VARIABILITY; HUMAN; MAJOR CLINICAL STUDY; MALE; MITOCHONDRION; NON INSULIN DEPENDENT DIABETES MELLITUS; PREVALENCE; CASE CONTROL STUDY; CAUCASIAN; GENETIC PREDISPOSITION; GENETICS; SINGLE NUCLEOTIDE POLYMORPHISM;

CASE-CONTROL STUDIES; CORONARY ARTERY DISEASE; DIABETES MELLITUS, TYPE 2; DNA, MITOCHONDRIAL; EUROPE; EUROPEAN CONTINENTAL ANCESTRY GROUP; GENETIC PREDISPOSITION TO DISEASE; HUMANS; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 79551505787     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0016455     Document Type: Article

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