NEXN Gene in Cardiomyopathies and Sudden Cardiac Deaths: Prevalence, Phenotypic Expression, and Prognosis.

doi:10.1161/CIRCGEN.123.004285

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Article

NEXN Gene in Cardiomyopathies and Sudden Cardiac Deaths: Prevalence, Phenotypic Expression, and Prognosis.

Circulation. Genomic and precision medicine - 1 Feb 2024

Hermida Alexis, Ader Flavie, Millat Gilles, Jedraszak Guillaume, Maury Phillipe, Cador Romain, Catalan Pierre-Antoine, Clerici Gaël, Combes Nicolas, De Groote Pascal, Dupin-Deguine Delphine, Eschalier Romain, Faivre Laurence, Garcia Patricia, Guillon Benoit, Janin Alexandre, Kugener Beatrice, Lackmy Marylin, Laredo Mikael, Le Guillou Xavier, Lesaffre François, Lucron Hugues, Milhem Antoine, Nadeau Gwenaël, Nguyen Karine, Palmyre Aurélien, Perdreau Elodie, Picard François, Rebotier Nicolas, Richard Pascale, Rooryck Caroline, Seitz Julien, Verloes Alain, Vernier Agathe, Winum Pierre, Yabeta Grace-A-Dieu, Bouchot Océane, Chevalier Philippe, Charron Philippe, Gandjbakhch Estelle

Abstract excerpt

BACKGROUND: Few clinical data are available on NEXN mutation carriers, and the gene's involvement in cardiomyopathies or sudden death has not been fully established. Our objectives were to assess the prevalence of putative pathogenic variants in NEXN and to describe the phenotype and prognosis of patients carrying the variants. METHODS: DNA samples from consecutive patients with cardiomyopathy or sudden cardiac...

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Identifiers

PMID: 38059363
DOI: 10.1161/CIRCGEN.123.004285

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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