Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations

✍ Scribed by Purevjav, E.; Arimura, T.; Augustin, S.; Huby, A.-C.; Takagi, K.; Nunoda, S.; Kearney, D. L.; Taylor, M. D.; Terasaki, F.; Bos, J. M.; Ommen, S. R.; Shibata, H.; Takahashi, M.; Itoh-Satoh, M.; McKenna, W. J.; Murphy, R. T.; Labeit, S.; Yamanaka, Y.; Machida, N.; Park, J.-E.; Alexander, P. M. A.; Weintraub, R. G.; Kitaura, Y.; Ackerman, M. J.; Kimura, A.; Towbin, J. A.

• Book ID: 125815153
• Publisher: Oxford University Press
• Year: 2012
• Tongue: English
• Weight: 959 KB
• Volume: 21
• Category: Article
• ISSN: 0964-6906
• DOI: 10.1093/hmg/dds022