Effect of KCNJ5 Mutations on Gene Expression in Aldosterone-Producing Adenomas and Adrenocortical Cells

CONTEXT: Primary aldosteronism is a heterogeneous disease that includes both sporadic and familial forms. A point mutation in the KCNJ5 gene is responsible for familial hyperaldosteronism type III. Somatic mutations in KCNJ5 also occur in sporadic aldosterone producing adenomas (APA). OBJECTIVE: The...

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Main Authors: Monticone, Silvia, Hattangady, Namita G., Nishimoto, Koshiro, Mantero, Franco, Rubin, Beatrice, Cicala, Maria Verena, Pezzani, Raffaele, Auchus, Richard J., Ghayee, Hans K., Shibata, Hirotaka, Kurihara, Isao, Williams, Tracy A., Giri, Judith G., Bollag, Roni J., Edwards, Michael A., Isales, Carlos M., Rainey, William E.
Formato: Artigo
Idioma:Inglês
Publicado em: Endocrine Society 2012
Assuntos:
JCEM Online: Advances in Genetics
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3410264/
https://ncbi.nlm.nih.gov/pubmed/22628608
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2011-3132
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