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Comment
. 2018 Apr;14(4):213.
doi: 10.1038/nrneph.2018.17. Epub 2018 Feb 26.

Hypertension: CLCN2 chloride channel mutations in primary aldosteronism

Comment

Hypertension: CLCN2 chloride channel mutations in primary aldosteronism

Susan J Allison. Nat Rev Nephrol. 2018 Apr.
No abstract available

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Comment on

  • CLCN2 chloride channel mutations in familial hyperaldosteronism type II.
    Scholl UI, Stölting G, Schewe J, Thiel A, Tan H, Nelson-Williams C, Vichot AA, Jin SC, Loring E, Untiet V, Yoo T, Choi J, Xu S, Wu A, Kirchner M, Mertins P, Rump LC, Onder AM, Gamble C, McKenney D, Lash RW, Jones DP, Chune G, Gagliardi P, Choi M, Gordon R, Stowasser M, Fahlke C, Lifton RP. Scholl UI, et al. Nat Genet. 2018 Mar;50(3):349-354. doi: 10.1038/s41588-018-0048-5. Epub 2018 Feb 5. Nat Genet. 2018. PMID: 29403011 Free PMC article.
  • A gain-of-function mutation in the CLCN2 chloride channel gene causes primary aldosteronism.
    Fernandes-Rosa FL, Daniil G, Orozco IJ, Göppner C, El Zein R, Jain V, Boulkroun S, Jeunemaitre X, Amar L, Lefebvre H, Schwarzmayr T, Strom TM, Jentsch TJ, Zennaro MC. Fernandes-Rosa FL, et al. Nat Genet. 2018 Mar;50(3):355-361. doi: 10.1038/s41588-018-0053-8. Epub 2018 Feb 5. Nat Genet. 2018. PMID: 29403012

References

    1. Nat Genet. 2018 Feb 5;:null - PubMed
    1. Nat Genet. 2018 Feb 5;:null - PubMed

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