Phenotypic Expression, Natural History and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants

Marta Gigli,Davide Stolfo,Sharon L. Graw,Marco Merlo,Caterina Gregorio,Suet Nee Chen,Matteo Dal Ferro,Alessia Paldino,Giulia De Angelis,Francesca Brun,Jean Jirikowic,Ernesto E. Salcedo,Sylvia Turja,Diane Fatkin,Renee Johnson,J. Peter van Tintelen,Anneline S.J.M. te Riele,Arthur A.M. Wilde,Neal K. Lakdawala,Kermshlise Picard,Daniela Miani,Daniele Muser,Giovanni Maria Severini,Hugh Calkins,Cynthia A. James,Brittney Murray,Crystal Tichnell,Victoria N. Parikh,Euan A. Ashley,Chloe M. Reuter,Jiangping Song,Daniel P. Judge,William J. McKenna,Matthew R.G. Taylor,Gianfranco Sinagra,Luisa Mestroni

Phenotypic Expression, Natural History and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants

2021

Background: Filamin C truncating variants (FLNCtv) cause a form of arrhythmogenic cardiomyopathy (ACM): the mode of presentation, natural history and risk stratification of FLNCtv remain incomplete...

Keywords:

Filamin
Phenotype
risk stratification
Genetics
Cardiomyopathy
Natural history
Medicine

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