J. Cavanaugh

Danon disease presenting with dilated cardiomyopathy and a complex phenotype

L. Mestroni, J. Towbin, M. Lovell, 2007, Journal of Human Genetics.

MUTATION SCREENING OF SARCOMERE GENES MYH7, MYBPC3, LDB3, AND TNNT2 IN A LARGE COHORT OF DILATED CARDIOMYOPATHY FAMILIES

L. Mestroni, E. Salcedo, Matthew R. G. Taylor, 2010 .

α-Myosin Heavy Chain: A Sarcomeric Gene Associated With Dilated and Hypertrophic Phenotypes of Cardiomyopathy

Pamela R. Fain, Michael R. Bristow, Gianfranco Sinagra, 2005 .

Discovery of a potentially deleterious variant in TMEM87B in a patient with a hemizygous 2q13 microdeletion suggests a recessive condition characterized by congenital heart disease and restrictive cardiomyopathy

T. Shaikh, Hung-Chun Yu, S. Miyamoto, 2016, Cold Spring Harbor molecular case studies.

Thymopoietin (lamina‐associated polypeptide 2) gene mutation associated with dilated cardiomyopathy

L. Mestroni, R. Foisner, P. Fain, 2005, Human mutation.

Prevalence of Desmin Mutations in Dilated Cardiomyopathy

C. Long, L. Mestroni, P. Lavori, 2007, Circulation.

Lower spatial QRS-T angle rules out sustained ventricular arrhythmias in children with hypertrophic cardiomyopathy

J. Alejos, J. Aboulhosn, S. Miyamoto, 2016, Cardiology in the Young.

Predicting recovery: successful explant of a ventricular assist device in a child with dilated cardiomyopathy.

Christine E. Peyton, D. Campbell, S. Miyamoto, 2010, The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation.

The spatial QRS-T angle outperforms the Italian and Seattle ECG-based criteria for detection of hypertrophic cardiomyopathy in pediatric patients.

Nandita Sharma, Todd T Schlegel, Keith Weiner, 2015, Journal of electrocardiology.