SNPs at the 3′ end of the angiotensinogen gene define two haplotypes associated with the common 235Met variant [3]

American Journal of Human Genetics

Volumn 71, Issue 2, 2002, Pages 443-444

  Plummer, S ^a   Morgan, L ^a   Kalsheker, N ^a  

^a NOTTINGHAM UNIVERSITY HOSPITALS NHS TRUST   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ANGIOTENSIN DERIVATIVE; ANGIOTENSINOGEN;

AMINO ACID SUBSTITUTION; GENETICS; HAPLOTYPE; HUMAN; NOTE; SINGLE NUCLEOTIDE POLYMORPHISM; AMINO ACID SEQUENCE; EXON; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; LETTER; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL;

AMINO ACID SUBSTITUTION; ANGIOTENSINS; HAPLOTYPES; HUMANS; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 0035984409     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/341721     Document Type: Letter

References (9)

1. Angiotensinogen as a risk factor for essential hypertension in Japan
2. Molecular basis of human hypertension: Role of angiotensinogen
3. Dinucleotide repeat polymorphism in the human angiotensinogen gene
4. DNA polymorphisms and linkage disequilibrium in the angiotensinogen gene
5. Polymorphism in oestrogen response element associated with variation in plasma angiotensinogen concentrations in healthy pregnant women
6. Nucleotide diversity and haplotype structure of the human angiotensinogen gene in two populations
7. Identification of cell type-dependent enhancer core element located in the 3′-downstream region of the human angiotensinogen gene
8. A cell type-dependent enhancer core element is located in exon 5 of the human angiotensinogen gene
9. A molecular variant of angiotensinogen associated with preeclampsia