@article{frutos2024clinical,
 abstract = {Background Although genetic variants in MYH7 are the most frequent cause of pediatric genetic dilated cardiomyopathy (DCM), there are no studies available describing this entity. We sought to describe clinical features, analyze variant location, and explore predictors of bad prognosis in pediatric MYH7‐related DCM. Methods and Results We evaluated clinical records from 44 patients (24 men; median age at diagnosis, 0.54 [interquartile range, 0.01–10.8] years) with pathogenic/likely pathogenic variants in MYH7 diagnosed with DCM at pediatric age (<18 years) followed at 13 international centers. ...},
 author = {F. Frutos and PhD Juan and MD Pablo Ochoa and Phil Webster and Mph Janice Mark Md and Priya Md and Maria Rasmussen and PhDHyunSunJeon Md and PhD Roberto Barriales-Villa and Priya Md and P. César and M. E. Fuentes-Cañamero and MD Reyes Alvarez García-Rovés and Miriam Wahbi and MD Javier Limeres and P. Kubanek and PhD Martijn G. Slieker and MD PhD Georgia Sarquella-Brugada and P. Abrams and M. Md and PhD Fernando Domínguez and Priya Md},
 doi = {10.1161/JAHA.124.036208},
 journal = {Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease},
 title = {Clinical Features and Outcomes of Pediatric MYH7‐Related Dilated Cardiomyopathy},
 volume = {13},
 year = {2024}
}