NEXN Gene in Cardiomyopathies and Sudden Cardiac Deaths: Prevalence, Phenotypic Expression, and Prognosis.
Alexis HermidaFlavie AderGilles MillatGuillaume JedraszakPhilippe MauryRomain CadorPierre Antoine CatalanGaël ClericiNicolas CombesPascal De GrooteDelphine Dupin-DeguineRomain EschalierLaurence Olivier-FaivrePatricia GarciaBenoit GuillonAlexandre JaninBeatrice KugenerMarylin LackmyMikael LaredoXavier Maximin Le Guillou HornFrançois LesaffreHugues LucronAntoine MilhemGwenaël NadeauKarine NguyenAsurélien PalmyreElodie PerdreauFrançois PicardNicolas RebotierPascale RichardCaroline RooryckJulien SeitzAlain VerloesAgathe VernierPierre WinumGrace-A-Dieu YabetaOcéane BouchotPhilippe ChevalierPhilippe CharronEstelle GandjbakhchPublished in: Circulation. Genomic and precision medicine (2023)
variants in patients with hypertrophic cardiomyopathy and sudden infant death syndrome/idiopathic ventricular fibrillation, although a causal link could not be established.