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B

Beuschlein, Felix and Boulkroun, Sheerazed and Osswald, Andrea and Wieland, Thomas and Nielsen, Hang N. and Lichtenauer, Urs D. and Penton, David and Schack, Vivien R. and Amar, Laurence and Fischer, Evelyn and Walther, Anett and Tauber, Philipp and Schwarzmayr, Thomas and Diener, Susanne and Graf, Elisabeth and Allolio, Bruno and Samson-Couterie, Benoit and Benecke, Arndt and Quinkler, Marcus and Fallo, Francesco and Plouin, Pierre-Francois and Mantero, Franco and Meitinger, Thomas and Mulatero, Paolo and Jeunemaitre, Xavier and Warth, Richard and Vilsen, Bente and Zennaro, Maria-Christina and Strom, Tim M. and Reincke, Martin (2013) Somatic mutations in ATP1A1 and ATP2B3 lead to aldosterone-producing adenomas and secondary hypertension. NATURE GENETICS, 45 (4). pp. 440-444. ISSN 1061-4036

K

Kleta, R. and Romeo, E. and Ristic, Z. and Ohura, T. and Stuart, C. and Arcos-Burgos, M. and Dave, M. H. and Wagner, C. A. and Camargo, S. R. M. and Inoue, S. and Matsuura, N. and Helip-Wooley, A. and Bockenhauer, D. and Warth, Richard and Bernardini, I. and Visser, G. and Eggermann, T. and Lee, P. and Chairoungdua, A. and Jutabha, P. and Babu, E. and Nilwarangkoon, S. and Anzai, N. and Kanai, Y. and Verrey, F. and Gahl, W. A. and Koizumi, A. (2004) Mutations in SLC6A19, encoding B(0)AT1, cause Hartnup disorder. NATURE GENETICS, 36 (9). pp. 999-1002. ISSN 1061-4036, 1546-1718