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KCNJ5 mutations in the National Institutes of Health cohort of patients with primary hyperaldosteronism: an infrequent genetic cause of Conn's syndrome.
Xekouki P, Hatch MM, Lin L, Rodrigo de A, Azevedo M, de la Luz Sierra M, Levy I, Saloustros E, Moraitis A, Horvath A, Kebebew E, Hoffman DA, Stratakis CA. Xekouki P, et al. Among authors: hoffman da. Endocr Relat Cancer. 2012 May 3;19(3):255-60. doi: 10.1530/ERC-12-0022. Print 2012 Jun. Endocr Relat Cancer. 2012. PMID: 22323562 Free PMC article.
DPP6 domains responsible for its localization and function.
Lin L, Long LK, Hatch MM, Hoffman DA. Lin L, et al. Among authors: hoffman da. J Biol Chem. 2014 Nov 14;289(46):32153-32165. doi: 10.1074/jbc.M114.578070. Epub 2014 Sep 4. J Biol Chem. 2014. PMID: 25190807 Free PMC article.
Functional characterization of two novel germline mutations of the KCNJ5 gene in hypertensive patients without primary aldosteronism but with ACTH-dependent aldosterone hypersecretion.
Sertedaki A, Markou A, Vlachakis D, Kossida S, Campanac E, Hoffman DA, Sierra ML, Xekouki P, Stratakis CA, Kaltsas G, Piaditis GP, Chrousos GP, Charmandari E. Sertedaki A, et al. Among authors: hoffman da. Clin Endocrinol (Oxf). 2016 Dec;85(6):845-851. doi: 10.1111/cen.13132. Epub 2016 Jul 12. Clin Endocrinol (Oxf). 2016. PMID: 27293068 Free PMC article.
111 results