(Q33698924)

English

KCNJ5 mutations in the National Institutes of Health cohort of patients with primary hyperaldosteronism: an infrequent genetic cause of Conn's syndrome

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Europe PubMed Central

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28 July 2017

KCNJ5 mutations in the National Institutes of Health cohort of patients with primary hyperaldosteronism: an infrequent genetic cause of Conn's syndrome (English)

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Europe PubMed Central

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28 July 2017

Conn's syndrome

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12

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Dax A Hoffman

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28 July 2017

Emmanouil Saloustros

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Emmanouil Saloustros

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Europe PubMed Central

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28 July 2017

Constantine A Stratakis

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Constantine A Stratakis

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28 July 2017

Electron Kebebew

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E Kebebew

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28 July 2017

Paraskevi Xekouki

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Paraskevi Xekouki

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28 July 2017

Monalisa Azevedo

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Monalisa Azevedo

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28 July 2017

Maria de la Luz Sierra

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Maria de la Luz Sierra

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10

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Anelia Horvath

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28 July 2017

author name string

Michael M Hatch

2

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28 July 2017

Lin Lin

3

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28 July 2017

De Alexandre Rodrigo

4

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28 July 2017

Isaac Levy

7

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28 July 2017

Andreas Moraitis

9

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28 July 2017

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publication date

3 May 2012

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28 July 2017

Endocrine-Related Cancer

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28 July 2017

19

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28 July 2017

3

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28 July 2017

255-260

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28 July 2017

Mutations in KCNJ5 gene cause hyperaldosteronism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4041522

21 June 2018

K+ channel mutations in adrenal aldosterone-producing adenomas and hereditary hypertension

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4041522

21 June 2018

Identification of a Kir3.4 mutation in congenital long QT syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4041522

21 June 2018

Heteromeric assembly of inward rectifier channel subunit Kir2.1 with Kir3.1 and with Kir3.4.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4041522

21 June 2018

Case detection, diagnosis, and treatment of patients with primary aldosteronism: an endocrine society clinical practice guideline

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4041522

21 June 2018

Primary aldosteronism: current knowledge and controversies in Conn's syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4041522

21 June 2018

Prevalence of primary hyperaldosteronism in resistant hypertension: a retrospective observational study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4041522

30 October 2018

Characterizations of a loss-of-function mutation in the Kir3.4 channel subunit.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4041522

30 October 2018

Increased diagnosis of primary aldosteronism, including surgically correctable forms, in centers from five continents.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4041522

30 October 2018

Molecular basis of ion selectivity, block, and rectification of the inward rectifier Kir3.1/Kir3.4 K(+) channel

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4041522

30 October 2018

Comparative genomic hybridization analysis of adrenocortical tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/22323562

12 December 2020

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Identifiers

10.1530/ERC-12-0022

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PMC publication ID

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Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

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