Mutations in KCNJ5 determines presentation and likelihood of cure in primary hyperaldosteronism.

Ip, Julian C Y

Mutations in KCNJ5 determines presentation and likelihood of cure in primary hyperaldosteronism. [electronic resource] - ANZ journal of surgery Apr 2015 - 279-83 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

1445-2197

10.1111/ans.12470 doi


Adrenal Cortex Neoplasms--complications
Adrenal Hyperplasia, Congenital--complications
Adrenalectomy
Adrenocortical Adenoma--complications
Adult
Aged
Aged, 80 and over
Australia
Cohort Studies
Female
G Protein-Coupled Inwardly-Rectifying Potassium Channels--genetics
Genetic Markers
Heterozygote
Humans
Hyperaldosteronism--diagnosis
Logistic Models
Male
Middle Aged
Mutation
Treatment Outcome