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Volumn 112, Issue 2, 2013, Pages 318-326

Effects of rare and common blood pressure gene variants on essential hypertension: Results from the family blood pressure program, CLUE, and atherosclerosis risk in communities studies

Author keywords

blood pressure; DNA sequencing; essential hypertension; genotype; population genetics

Indexed keywords

AGT GENE; ARTICLE; ATHEROSCLEROSIS; CYP11B1 GENE; CYP17A1 GENE; DIASTOLIC BLOOD PRESSURE; DNA SEQUENCE; ESSENTIAL HYPERTENSION; ETHNICITY; GENE; GENE FREQUENCY; GENE LOCUS; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPING TECHNIQUE; HSD11B2 GENE; HUMAN; MAJOR CLINICAL STUDY; MISSENSE MUTATION; NR3C1 GENE; NR3C2 GENE; PRIORITY JOURNAL; RISK ASSESSMENT; SCNN1A GENE; SCNN1B GENE; SCNN1G GENE; SYSTOLIC BLOOD PRESSURE; WNK1 GENE; WNK4 GENE;

EID: 84872844633     PISSN: 00097330     EISSN: 15244571     Source Type: Journal    
DOI: 10.1161/CIRCRESAHA.112.276725     Document Type: Article
Times cited : (19)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.