A Novel Y152C KCNJ5 Mutation Responsible for Familial Hyperaldosteronism Type III

CONTEXT: Primary aldosteronism is a heterogeneous group of disorders comprising both sporadic and familial forms. Mutations in the KCNJ5 gene, which encodes the inward rectifier K(+) channel 4 (G protein-activated inward rectifier K(+) channel 4, Kir3.4), cause familial hyperaldosteronism type III (...

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Main Authors: Monticone, Silvia, Hattangady, Namita G., Penton, David, Isales, Carlos M., Edwards, Michael A., Williams, Tracy A., Sterner, Christina, Warth, Richard, Mulatero, Paolo, Rainey, William E.
Formato: Artigo
Idioma:Inglês
Publicado em: Endocrine Society 2013
Assuntos:
JCEM Online: Advances in Genetics
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3816265/
https://ncbi.nlm.nih.gov/pubmed/24037882
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2013-2428
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