Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations.
Purevjav, Enkhsaikhan; Arimura, Takuro; Augustin, Sibylle; Huby, Anne-Cecile; Takagi, Ken; Nunoda, Shinichi; Kearney, Debra L.; Taylor, Michael D.; Terasaki, Fumio; Bos, Johan M.; Ommen, Steve R.; Shibata, Hiroki; Takahashi, Megumi; Itoh-Satoh, Manatsu; McKenna, William J.; Murphy, Ross T.; Labeit, Siegfried; Yamanaka, Yoichi; Machida, Noboru; Park, Jeong-Euy; Human Molecular Genetics, 2012, vol. 21, issue 9, p 2039, ISSN 09646906. ISBN 14602083.

Full Text Resources Located for this Citation

View article on EBSCOhost(Login required)
View article via CrossRef