Citations for
1CYP11B2, GSH
Five novel mutations in CYP11B2 gene detected in patients with aldosterone synthase deficiency type I: Functional characterization and structural analyses.
Nguyen HH, Hannemann F, Hartmann MF, Malunowicz EM, Wudy SA, Bernhardt R.
Mol Genet Metab 100(4):357-64. Epub 2010 May 21.PMID: 20494601 2010
2CYP11B1, GSH
A novel form of human mendelian hypertension featuring nonglucocorticoid-remediable aldosteronism.
Geller DS, Zhang J, Wisgerhof MV, Shackleton C, Kashgarian M, Lifton RP.
J Clin Endocrinol Metab 93(8):3117-23. Epub 2008 May 27.PMID: 18505761 2008
3FHA2, GSH, CYP11B2
New genetic insights in familial hyperaldosteronism.
Jackson RV, Lafferty A, Torpy DJ, Stratakis C.
Ann N Y Acad Sci 970:77-88. Review. 2002
4CYP11B1, CYP11B2, GSH
A chimaeric 11 beta-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension.
Lifton RP, et al.
Nature 355 : 262-265. 1992
5CYP11B1, CYP11B2, GSH
Hereditary hypertension caused by chimaeric gene duplications and ectopic expression of aldosterone synthase.
Lifton RP, et al.
Nat Genet 2 : 66-74. 1992
6GSH, CYP11B1, CYP11B2
The chimeric gene linked to glucocorticoid-suppressible hyperaldosteronism encodes a fused P-450 protein possessing aldosterone synthase activity.
Miyahara K, et al.
Biochem Biophys Res Commun 189 : 885-891. 1992
7CYP11B2, GSH
Hypertension, increased aldosterone secretion and low plasma renin activity relieved by dexamethasone.
Sutherland DJ, et al.
Can Med Assoc J 95 : 1109-1119. 1966