Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations.
Purevjav E; Arimura T; Augustin S; Huby AC; Takagi K; Nunoda S; Kearney DL; Taylor MD; Terasaki F; Bos JM; Ommen SR; Shibata H; Takahashi M; Itoh-Satoh M; McKenna WJ; Murphy RT; Labeit S; Yamanaka Y; Machida N; Park JE; Alexander PM; Weintraub RG; Kitaura Y; Ackerman MJ; Kimura A; Towbin JA; Human Molecular Genetics, 2012, vol. 21, issue 9, p 2039, ISSN 14602083. ISBN 14602083.

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