Abstract
Germline mutations in the chloride channel gene CLCN2 have been described as cause of familial hyperaldosteronism type II. In this issue, Dutta and colleagues in a groundbreaking study identify a somatic (tumor-specific) CLCN2 mutation in an aldosterone-producing adenoma, expanding the disease spectrum associated with CLCN2 mutations.
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CITATION STYLE
APA
Scholl, U. I. (2019). Clcn2 clicks with aldosterone-producing adenomas, too! European Journal of Endocrinology. BioScientifica Ltd. https://doi.org/10.1530/EJE-19-0688
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