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Article

Clinical and genetic characteristics of the patients with hypertension and hypokalemia carrying a novel SCNN1A mutation.

Scandinavian journal of clinical and laboratory investigation - 1 Jan 2000

Chen Mengzi, Lv Xi, Li Jiwu, Guo Manli, Ma Shaogang

Abstract excerpt

The objective of this study was to clinically and genetically characterize a pedigree with Liddle syndrome (LS). A LS pedigree comprising with one proband and seven family members was enrolled. The subjects' symptoms, laboratory results and genotypes were analyzed. Peripheral venous samples were collected from the subjects, and genomic DNA was extracted. DNA library construction and exome capture were performed...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 36336351
DOI: 10.1080/00365513.2022.2140454

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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