Hypertension genetics, single nucleotide polymorphisms, and the common disease: Common variant hypothesis

Hypertension

Volumn 39, Issue 2 II, 2002, Pages 323-331

  Doris, Peter A ^a  

^a UNIVERSITY OF TEXAS MEDICAL SCHOOL   (United States)

Author keywords

Epidemiology; Genes; Hypertension, essential; Polymorphism

Indexed keywords

11BETA HYDROXYSTEROID DEHYDROGENASE; ANGIOTENSIN 2 RECEPTOR; APOLIPOPROTEIN E; BRADYKININ RECEPTOR; CYTOCHROME P450; DOPAMINE; DOPAMINE RECEPTOR; INSULIN RECEPTOR; LOW DENSITY LIPOPROTEIN RECEPTOR; MINERALOCORTICOID; MINERALOCORTICOID RECEPTOR; MITOCHONDRIAL DNA; NITRIC OXIDE SYNTHASE; PHOSPHOPROTEIN; PROTEIN TYROSINE PHOSPHATASE; STEROID 17ALPHA MONOOXYGENASE;

ALLELE; CHROMOSOME; CONFERENCE PAPER; DISEASE PREDISPOSITION; ESSENTIAL HYPERTENSION; GENE; GENE CONVERSION; GENE LINKAGE DISEQUILIBRIUM; GENETIC HETEROGENEITY; GENETIC SUSCEPTIBILITY; GENOTYPE; HUMAN; HYPOTHESIS; INHERITANCE; MASS SPECTROMETRY; NONHUMAN; PHENOTYPE; PHYLOGENY; POLYMERASE CHAIN REACTION; PREVALENCE; PRIORITY JOURNAL; QUANTITATIVE TRAIT LOCUS; SINGLE NUCLEOTIDE POLYMORPHISM;

ALLELES; EVOLUTION, MOLECULAR; GENE CONVERSION; GENETIC PREDISPOSITION TO DISEASE; HUMANS; HYPERTENSION; LINKAGE DISEQUILIBRIUM; MODELS, GENETIC; POLYMORPHISM, SINGLE NUCLEOTIDE; RECOMBINATION, GENETIC;

EID: 0036179423     PISSN: 0194911X     EISSN: None     Source Type: Journal    
DOI: 10.1161/hy0202.104087     Document Type: Conference Paper

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