Hypertrophic cardiomyopathy due to truncating variants in myosin binding protein C: a Spanish cohort

Hypertrophic cardiomyopathy due to truncating variants in myosin binding protein C: a Spanish cohort

Background Hypertrophic cardiomyopathy (HCM) is an inherited disorder whose causal variants involve sarcomeric protein genes. One of these is myosin-binding protein C (MYBPC3), being previously associated with a favourable prognosis. Our objective is to describe the clinical characteristics and even...

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Main Authors: Carles Díez-López, María Luisa Peña-Peña, Hector Bueno, Fernando Arribas Ynsaurriaga, Vicente Climent-Payá, Maria Melendo-Viu, Rafael Salguero-Bodes, María Valverde-Gómez, Jose María Larrañaga-Moreira, Roberto Barriales, Javier Limeres Freire, Pablo Garcia Pavia, Tomas Ripoll, Maria Gallego Delgado, Esther Zorio, Francisco José Bermudez Jimenez, José Manuel García-Pinilla, Irene Méndez Fernández, Maria Sabater-Molina, Ana Perez Asensio, Álvaro Marchán-Lopez, Julián A Palomino Doza
Format: Article
Language:English
Published: BMJ Publishing Group 2024-12-01
Series:Open Heart
Online Access:https://openheart.bmj.com/content/11/2/e002891.full
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https://openheart.bmj.com/content/11/2/e002891.full

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