Haplotype analysis in human hypertension

Journal of Hypertension

Volumn 23, Issue 4, 2005, Pages 711-712

  Manunta, Paolo ^a,c   Tripodi, Grazia ^b  

^a VITA SALUTE SAN RAFFAELE UNIVERSITY   (Italy)

^b Prassis Sigma Tau Research Institute   (Italy)

^c SAN RAFFAELE HOSPITAL   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

NITRIC OXIDE; NITRIC OXIDE SYNTHASE;

ALLELISM; BLOOD PRESSURE REGULATION; DNA SEQUENCE; EDITORIAL; GENE; GENETIC VARIABILITY; HAPLOTYPE; HUMAN; HYPERTENSION; NOS3 GENE; PATHOGENESIS; PRIORITY JOURNAL; SHORT TANDEM REPEAT; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 17144412999     PISSN: 02636352     EISSN: None     Source Type: Journal    
DOI: 10.1097/01.hjh.0000163135.69643.e4     Document Type: Editorial

References (4)

1. International Human Genome Sequencing Consortium. Finishing the euchromatic sequence of the human genome. Nature 2004; 431: 931-945.
2. Zhao H, Pfeiffer R, Gail MH. Haplotype analysis in population genetics and association studies. Pharmacogenomics 2003; 4:171-178.
3. The International HapMap Consortium. The International HapMap Project. Nature 2003; 426:789-796.
4. Persu A, Vink WJ, El Khattabi O, Janssen RGJH, Paulussen ADC, Devuyst O, et al. Influence of the endothelial nitric oxide synthase gene on conventional and ambulatory blood pressure: sib-pair analysis and haplotype study. J Hypertens 2005; 23:759-765.