The genetics of primary aldosteronism

Science

Volumn 331, Issue 6018, 2011, Pages 685-686

  Funder, John W ^a  

^a MONASH MEDICAL CENTRE   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ALDOSTERONE; ANGIOTENSIN 1 RECEPTOR; GLUCOCORTICOID; INWARDLY RECTIFYING POTASSIUM CHANNEL; POTASSIUM CHANNEL; G PROTEIN COUPLED INWARDLY RECTIFYING POTASSIUM CHANNEL; KCNJ5 PROTEIN, HUMAN;

GENOMICS; MUTATION; POTASSIUM; STEROID; TUMOR;

ADRENAL TUMOR; CHROMOSOME 7; CIRCADIAN RHYTHM; ELECTROPHYSIOLOGY; ESSENTIAL HYPERTENSION; GENE DELETION; GENE MUTATION; GENETIC ANALYSIS; GENETICS; HUMAN; NONHUMAN; PHENOTYPE; POTASSIUM EXCRETION; PRIMARY HYPERALDOSTERONISM; PRIORITY JOURNAL; SHORT SURVEY; SODIUM RETENTION; TUMOR VOLUME; ADRENAL CORTEX ADENOMA; ADRENAL CORTEX TUMOR; ADRENAL GLAND; ANIMAL; DISEASE MODEL; FEMALE; HYPERALDOSTERONISM; HYPERPLASIA; HYPERTENSION; MALE; METABOLISM; MOUSE; MUTATION; NOTE; PATHOLOGY; PATHOPHYSIOLOGY;

ADRENAL CORTEX NEOPLASMS; ADRENAL GLANDS; ADRENOCORTICAL ADENOMA; ALDOSTERONE; ANIMALS; DISEASE MODELS, ANIMAL; FEMALE; G PROTEIN-COUPLED INWARDLY-RECTIFYING POTASSIUM CHANNELS; HUMANS; HYPERALDOSTERONISM; HYPERPLASIA; HYPERTENSION; MALE; MICE; MUTATION;

EID: 79951501330     PISSN: 00368075     EISSN: 10959203     Source Type: Journal    
DOI: 10.1126/science.1202887     Document Type: Short Survey

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