A novel genetic locus for low renin hypertension: familial hyperaldosteronism type II maps to chromosome 7 (7p22) (Q24681542)

Familial hyperaldosteronism

inferred from title

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A R Lafferty

1

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D J Torpy

2

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M Stowasser

3

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S E Taymans

4

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J P Lin

5

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P Huggard

6

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R D Gordon

7

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C A Stratakis

Journal of Medical Genetics

8

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language of work or name

English

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publication date

November 2000

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published in

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volume

37

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issue

11

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page(s)

831-5

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A genetic defect resulting in mild low-renin hypertension

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The Product of the CYP11B2 Gene Is Required for Aldosterone Biosynthesis in the Human Adrenal Cortex

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A chimaeric llβ-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension

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Artificial mutations in P450c11AS (aldosterone synthase) can increase enzymatic activity: a model for low-renin hypertension?

28 July 2018

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High incidence of primary aldosteronism in 199 patients referred with hypertension

28 November 2018

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12 December 2020

Primary aldosteronism

1 reference

12 December 2020

A radiation hybrid map of the human genome

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12 December 2020

A PCR-based method of screening individuals of all ages, from neonates to the elderly, for familial hyperaldosteronism type I

1 reference

12 December 2020

Familial hyperaldosteronism type II: five families with a new variety of primary aldosteronism

1 reference

12 December 2020

Linkage analysis of familial hyperaldosteronism type II--absence of linkage to the gene encoding the angiotensin II receptor type 1

1 reference

12 December 2020

Familial hyperaldosteronism type II: description of a large kindred and exclusion of the aldosterone synthase (CYP11B2) gene

1 reference

12 December 2020