CLCN2 Chloride Channel Mutations in Familial Hyperaldosteronism Type II

Primary aldosteronism, a common cause of severe hypertension(1), features constitutive production of the adrenal steroid aldosterone. We analyzed a multiplex family with familial hyperaldosteronism type II (FH-II)(2) and 80 additional probands with unsolved early-onset primary aldosteronism. Eight p...

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Publicado no:Nat Genet
Main Authors: Scholl, Ute I., Stölting, Gabriel, Schewe, Julia, Thiel, Anne, Tan, Hua, Nelson-Williams, Carol, Vichot, Alfred A., Jin, Sheng Chih, Loring, Erin, Untiet, Verena, Yoo, Taekyeong, Choi, Jungmin, Xu, Shengxin, Wu, Aihua, Kirchner, Marieluise, Mertins, Philipp, Rump, Lars C., Onder, Ali Mirza, Gamble, Cory, McKenney, Daniel, Lash, Robert W., Jones, Deborah P., Chune, Gary, Gagliardi, Priscila, Choi, Murim, Gordon, Richard, Stowasser, Michael, Fahlke, Christoph, Lifton, Richard P.
Formato: Artigo
Idioma:Inglês
Publicado em: 2018
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5862758/
https://ncbi.nlm.nih.gov/pubmed/29403011
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41588-018-0048-5
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