A gain-of-function mutation in the CLCN2 chloride channel gene causes primary aldosteronism-Reference-Cited by-同舟云学术

A gain-of-function mutation in the CLCN2 chloride channel gene causes primary aldosteronism

Published:2018-02-05 Issue:3 Volume:50 Page:355-361
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Fernandes-Rosa Fabio L.^ORCID,Daniil Georgios,Orozco Ian J.,Göppner Corinna,El Zein Rami,Jain Vandana,Boulkroun Sheerazed,Jeunemaitre Xavier^ORCID,Amar Laurence,Lefebvre Hervé,Schwarzmayr Thomas,Strom Tim M.,Jentsch Thomas J.^ORCID,Zennaro Maria-Christina^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/s41588-018-0053-8.pdf

Reference43 articles.

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2. Jordt, S. E. & Jentsch, T. J. Molecular dissection of gating in the ClC-2 chloride channel. EMBO J. 16, 1582–1592 (1997).

3. Gründer, S., Thiemann, A., Pusch, M. & Jentsch, T. J. Regions involved in the opening of CIC-2 chloride channel by voltage and cell volume. Nature 360, 759–762 (1992).

4. NCD Risk Factor Collaboration (NCD-RisC). Worldwide trends in blood pressure from 1975 to 2015: a pooled analysis of 1479 population-based measurement studies with 19·1 million participants. Lancet 389, 37–55 (2017).

5. Hannemann, A. & Wallaschofski, H. Prevalence of primary aldosteronism in patient’s cohorts and in population-based studies—a review of the current literature. Horm. Metab. Res. 44, 157–162 (2012).

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