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Dominiczak AF, Negrin DC, Clark JS, Brosnan MJ, McBride MW, Alexander MY . Genes and hypertension: from gene mapping in experimental models to vascular gene transfer strategies. Hypertension 2000; 35: 164–172.
Colhoun H . Confirmation needed for genes for hypertension. Lancet 1999; 353: 1200–1201.
Shi NQ, Ye B, Makielski JC . Function and distribution of the SUR isoforms and splice variants. J Mol Cell Cardiol 2005; 39: 51–60.
Gong M, Zhang H, Schulz H, Lee YA, Sun K, Bahring S . Genome-wide linkage reveals a locus for human essential (primary) hypertension on chromosome 12p. Hum Mol Genet 2003; 12: 1273–1277.
Chutkow WA, Pu J, Wheeler MT, Wada T, Makielski JC, Burant CF et al. Episodic coronary artery vasospasm and hypertension develop in the absence of Sur2 K(ATP) channels. J Clin Invest 2002; 110: 203–208.
Nakayama T, Soma M, Kanmatsuse K, Kokubun S . The microsatellite alleles on chromosome 1 associated with essential hypertension and blood pressure levels. J Hum Hypertens 2004; 18: 823–828.
Kobayashi Y, Nakayama T, Sato N, Izumi Y, Kokubun S, Soma M . Haplotype-based case–control study of Adrenomedullin genes on Proteinuria in the subjects with Essential Hypertension. Hypertens Res 2005; 28: 229–236.
Dempster AP, Laird NM, Rubin DB . Maximum likelihood from in complete data via the EM algorithm. J R Stat Soc 1977; 39: 1–22.
Morris RW, Kaplan NL . On the advantage of haplotype analysis in the presence of multiple disease susceptibility alleles. Genet Epidemiol 2002; 23: 221–233.
Sharma P, Hingorani A, Jia H, Hopper R, Brown MJ . Quantitative association between a newly identified molecular variant in the endothelin-2 gene and human essential hypertension. J Hypertens 1999; 7: 1281–1287.
Ombra MN, Forabosco P, Casula S, Angius A, Maestrale G, Petretto E . Identification of a new candidate locus for uric acid nephrolithiasis. Am J Hum Genet 2001; 68: 1119–1129.
Bahring S, Rauch A, Toka O, Schroeder C, Hesse C, Siedler H et al. Autosomal-dominant hypertension with type E brachydactyly is caused by rearrangement on the short arm of chromosome 12. Hypertension 2004; 43: 471–476.
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Sato, N., Nakayama, T., Asai, S. et al. A haplotype in the human Sur2 gene is associated with essential hypertension. J Hum Hypertens 20, 87–90 (2006). https://doi.org/10.1038/sj.jhh.1001943
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DOI: https://doi.org/10.1038/sj.jhh.1001943
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