Mutations in KCNJ5 determines presentation and likelihood of cure in primary hyperaldosteronism. [electronic resource]
Producer: 20151222Description: 279-83 p. digitalISSN:- 1445-2197
- 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
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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