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The Journal of Physiology|February 9, 2011
Altered electroretinograms in patients with KCNJ10 mutations and EAST syndromeDorothy A Thompson, Sally Feather, Horia C Stanescu, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 24, 2010
KCNJ10 gene mutations causing EAST syndrome (epilepsy, ataxia, sensorineural deafness, and tubulopathy) disrupt channel functionMarkus Reichold, Anselm A Zdebik, Evelyn Lieberer, et al.
Hypertension (Dallas, Tex. : 1979)|March 5, 2014
Diastrophic dysplasia sulfate transporter (SLC26A2) is expressed in the adrenal cortex and regulates aldosterone secretionAriadni Spyroglou, Tarik Bozoglu, Rajesh Rawal, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 6, 2010
Task2 potassium channels set central respiratory CO2 and O2 sensitivityChristian Gestreau, Dirk Heitzmann, Joerg Thomas, et al.
Hypertension (Dallas, Tex. : 1979)|October 2, 2013
Somatic ATP1A1, ATP2B3, and KCNJ5 mutations in aldosterone-producing adenomasTracy Ann Williams, Silvia Monticone, Vivien R Schack, et al.
The EMBO Journal|November 24, 2007
Invalidation of TASK1 potassium channels disrupts adrenal gland zonation and mineralocorticoid homeostasisDirk Heitzmann, Renaud Derand, Stefan Jungbauer, et al.
Nature Genetics|September 14, 2023
Somatic SLC30A1 mutations altering zinc transporter ZnT1 cause aldosterone-producing adenomas and primary aldosteronismJuilee Rege, Sascha Bandulik, Kazutaka Nanba, et al.
Hypertension (Dallas, Tex. : 1979)|August 7, 2025
Somatic Mutations in <i>MCOLN3</i> Are Associated With Aldosterone-Producing AdenomasDesmaré van Rooyen, Sascha Bandulik, Grace A Coon, et al.
Hypertension (Dallas, Tex. : 1979)|December 29, 2011
KCNJ5 mutations in European families with nonglucocorticoid remediable familial hyperaldosteronismPaolo Mulatero, Philipp Tauber, Maria-Christina Zennaro, et al.
American Journal of Human Genetics|November 3, 2018
Germline De Novo Mutations in ATP1A1 Cause Renal Hypomagnesemia, Refractory Seizures, and Intellectual DisabilityKarl P Schlingmann, Sascha Bandulik, Cherry Mammen, et al.
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