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1
Journal Article
CLCN2 chloride channel mutations in familial hyperaldosteronism type II
Scholl, Ute I.
2018
Nature genetics, 50 (2018) 3, S. 349-354
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2
Journal Article
Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism
Scholl, Ute I
2015
eLife, 4 (2015) S. e06315
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Thiel
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Choi, Murim
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