Purevjav, E., & Labeit, S. (2012). Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations. Human molecular genetics, 21(9), . https://doi.org/10.1093/hmg/dds022
Chicago Style (17th ed.) CitationPurevjav, Enkhsaikhan, and Siegfried Labeit. "Molecular Basis for Clinical Heterogeneity in Inherited Cardiomyopathies Due to Myopalladin Mutations." Human Molecular Genetics 21, no. 9 (2012). https://doi.org/10.1093/hmg/dds022.
MLA (9th ed.) CitationPurevjav, Enkhsaikhan, and Siegfried Labeit. "Molecular Basis for Clinical Heterogeneity in Inherited Cardiomyopathies Due to Myopalladin Mutations." Human Molecular Genetics, vol. 21, no. 9, 2012, https://doi.org/10.1093/hmg/dds022.
Warning: These citations may not always be 100% accurate.