Mutated KCNJ5 activates the acute and chronic regulatory steps in aldosterone production

Article

Abstract: Somatic and germline mutations in the inward-rectifying K+ channel (KCNJ5) are a common cause of pri

Palabras claves:

Adrenal, aldosterone, KCNJ5 mutations, Primary aldosteronism (PA)

Autores:

Else T., Gomez-Sanchez C.E., Hattangady N.G., Jalife J., Karashima S., Ponce-Balbuena D., Rainey W.E., Richard J. Auchus, Yuan L.

Fuentes:

scopus