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Article

Further study of chromosome 7p22 to identify the molecular basis of familial hyperaldosteronism type II.

Journal of human hypertension - 1 Sept 2011

Carss K J, Stowasser M, Gordon R D, O'Shaughnessy K M

Abstract excerpt

Familial hyperaldosteronism type II (FH-II) is an inherited form of hyperaldosteronism associated with hypertension in most patients. The mutations that cause FH-II are unknown, but linkage analysis has mapped them to chromosome 7p22. As FH-II is clinically indistinguishable from sporadic primary...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 20927129
DOI: 10.1038/jhh.2010.93

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20927129-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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