Association of genetic variation in the mitochondrial genome with blood pressure and metabolic traits

Hypertension

Volumn 60, Issue 4, 2012, Pages 949-956

  Liu, Chunyu ^a,b   Yang, Qiong ^c   Hwang, Shih Jen ^a,b   Sun, Fengzhu ^d   Johnson, Andrew D ^a,b   Shirihai, Orian S ^e   Vasan, Ramachandran S ^a,e   Levy, Daniel ^a,b,e   Schwartz, Faina ^e  

^a FRAMINGHAM HEART STUDY   (United States)

^b NATIONAL HEART LUNG AND BLOOD INSTITUTE   (United States)

^c BOSTON UNIVERSITY SCHOOL OF PUBLIC HEALTH   (United States)

^d UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

^e BOSTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Association Study; diabetes mellitus; genetics; hypertension; Mitochondrial Genome

Indexed keywords

ALANINE; ASPARAGINE; ASPARTIC ACID; CYTOCHROME C OXIDASE; GLUCOSE; MITOCHONDRIAL DNA; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE); THREONINE;

ADULT; ARTICLE; BLOOD PRESSURE; BODY MASS; CLINICAL ARTICLE; DIABETES MELLITUS; DIET RESTRICTION; FOLLOW UP; GENE FREQUENCY; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE; GLUCOSE BLOOD LEVEL; HUMAN; HYPERTENSION; OBESITY; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; SYSTOLIC BLOOD PRESSURE;

ADULT; ALLELES; BLOOD PRESSURE; DNA, MITOCHONDRIAL; FEMALE; GENETIC ASSOCIATION STUDIES; GENOME, MITOCHONDRIAL; GENOTYPE; HUMANS; HYPERTENSION; MALE; MIDDLE AGED; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 84866538032     PISSN: 0194911X     EISSN: 15244563     Source Type: Journal    
DOI: 10.1161/HYPERTENSIONAHA.112.196519     Document Type: Article

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