Discerning the Ambiguous Role of Missense TTN Variants in Inherited Arrhythmogenic Syndromes

Martinez-Barrios, E; Sarquella-Brugada, G; Perez-Serra, A; Fernandez-Falgueras, A; Cesar, S; Coll, M; Puigmule, M; Iglesias, A; Alcalde, M; Vallverdu-Prats, M; Ferrer-Costa, C; del Olmo, B; Pico, F; Lopez, L; Fiol, V; Cruzalegui, J; Hernandez, C; Arbelo, E; Grassi, S; Oliva, A; Toro, R; Brugada, J; Brugada, R; Campuzano, O

Brugada, R; Campuzano, O (通讯作者),Univ Girona, Sch Med, Med Sci Dept, Girona 17003, Spain.;Brugada, R; Campuzano, O (通讯作者),Univ Girona, Cardiovasc Genet Ctr, IDIBGI, Girona 17190, Spain.;Brugada, R; Campuzano, O (通讯作者),Ctr Invest Biomed Red Enfermedades Cardiovasc CIB, Madrid 28029, Spain.;Brugada, R (通讯作者),Univ Girona, Hosp Josep Trueta, Cardiol Serv, Girona 17007, Spain.

JOURNAL OF PERSONALIZED MEDICINE, 2022; 12 (2):

Abstract

The titin gene (TTN) is associated with several diseases, including inherited arrhythmias. Most of these diagnoses are attributed to rare TTN variants......

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