Vol 1 No 1 (2011)

Published: 2011-08-23

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Tafazzin gene mutations are uncommon causes of dilated cardiomyopathy in adults

Matthew Taylor, Dobromir Slavov, Ernesto Salcedo, Xiao Zhu, Deborah Ferguson, Jean Jirikowic, Andrea Di Lenarda, Gianfranco Sinagra, Luisa Mestroni

Matrix metalloproteinase 9 polymorphism and outcome after myocardial infarction

Sophie Rodius, Guillermo Mulliert, Francisco Azuaje, Yvan Devaux, Daniel R. Wagner

LQTS-associated mutation A257G in α1-syntrophin interacts with the intragenic variant P74L to modify its biophysical phenotype

Jianding Cheng, David W. Van Norstrand, Argelia Medeiros-Domingo, David J. Tester, Carmen R. Valdivia, Bi-Hua Tan, Matteo Vatta, Jonathan C. Makielski, Michael J. Ackerman

Familial dilated cardiomyopathy associated with congenital defects in the setting of a novel VCL mutation (Lys815Arg) in conjunction with a known MYPBC3 variant

Quinn S. Wells, Natalie L. Ausborn, Birgit H. Funke, Jean P. Pfotenhauer, Joseph L. Fredi, Samantha Baxter, Thomas G. DiSalvo, Charles C. Hong

DNA variation in myoMIRs of the 1, 133, and 208 families in hypertrophic cardiomyopathy

María Palacín, Eliecer Coto, Julián R. Reguero, María Martín, César Morís, Belén Alonso, Marta Díaz, Ana I. Corao, Victoria Alvarez