Functional characterization of two novel germline mutations of the KCNJ5 gene in hypertensive patients without Primary Aldosteronism but with ACTH-dependent aldosterone hypersecretion

BACKGROUND: Germline mutations of the KCNJ5 gene encoding Kir3.4, a member of the inwardly rectifying K(+) channel, have been identified in “normal” adrenal glands, patients with Familial Hyperaldosteronism (FH) type III, aldosterone-producing adenomas (APAs) and sporadic cases of primary aldosteron...

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Publicado no:Clin Endocrinol (Oxf)
Principais autores: Sertedaki, Amalia, Markou, Athina, Vlachakis, Dimitrios, Kossida, Sophia, Campanac, Emilie, Hoffman, Dax A., De La Luz Sierra, Maria, Xekouki, Paraskevi, Stratakis, Constantine A., Kaltsas, Gregory, Piaditis, George P., Chrousos, George P., Charmandari, Evangelia
Formato: Artigo
Idioma:Inglês
Publicado em: 2016
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5118167/
https://ncbi.nlm.nih.gov/pubmed/27293068
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cen.13132
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