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2. Functional and clinical characterization of a novel homozygous KCNH2 missense variant in the pore region of Kv11.1 leading to a viable but severe long-QT syndrome. Delinière A; Jaupart L; Janin A; Millat G; Boulin T; Andrini O; Chevalier P Gene; 2024 Mar; 897():148076. PubMed ID: 38086455 [TBL] [Abstract][Full Text] [Related]
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