1Lifton RP, Dluhy RG, Powers M, et al. A chimaeric 1β-hydroxylase/aldosterone synthase gene causes glucocorticoid remediable aldosteronismand human hypertension. Nature, 1992, 355:262.
2Shimkets RA, Warnock DG, Bositis CM, et al. Liddle's syndrome.. Heritable human hypertension caused by mutations in the β subunit of the epithelial sodium channel. Cell, 1994,79: 407.
3Hansson JH, Nelson-Williams C, Suzuki H, et al. Hypertension caused by a truncated epithelial sodium channel gamma subunit: genetic heterogeneity of giddle syndrome. Nat Genet, 1995,11 : 76.
5Knight KK, Olson DR, Zhou R, et al. Liddle's syndrome mutations increase Na^+ transport through dual effects on epithelial Na^+ channel surface expression and proteolytic cleavage. Proc Natl Acad Sci USA, 2006,103 : 2805.
6Mune T, Rogerson FM, Nikkilg H, et al. Human hypertension caused by mutations in the kidney isozyme of 11β-hydroxysteroid dehydrogenase. Nat Genet, 1995,10 : 394.
7Atanasov AG, Ignatova ID, Nashev LG, et al. Impaired protein stability of 11beta-hydroxysteroid dehydrogenase type 2: a novel mechanism of apparent mineraloeorticoid excess. J Am Soc Nephrol, 2007,18 : 1262.
8Geller DS, Farhi A, Pinkerton N, et al. Activating mineralocortieoid receptor mutation in hypertension exacerbated by pregnancy. Science, 2000,289 : 119.
9Wilson FH, Disse-Nicodeme S, Choate KA, et al. Human hypertension caused by mutations in WNK kinases. Science,2001, 293:1107.
10Xu B, Stippec S, Chu P-Y, et al. WNKI activates SGKI to regulate the epithelial sodium channel. Proc Natl Acad Sci USA, 2005, 102:10315.
