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KLHL3 mutations cause familial hyperkalemic hypertension ... | ResearchHub
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KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron
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Authors
Hélène Louis-Dit-Picard
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Hélène Louis-Dit-Picard
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Olena Pylypenko
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•
Xavier Jeunemaı̂tre
Published
March 11, 2012
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Journal
Nature Genetics
Topics
Biology
Internal Medicine
Chemistry
Medicine
Endocrinology
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DOI
10.1038/ng.2218