Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies.

MLA

Arimura, Takuro, et al. “Mouse Model Carrying H222P-Lmna Mutation Develops Muscular Dystrophy and Dilated Cardiomyopathy Similar to Human Striated Muscle Laminopathies.” Human Molecular Genetics, vol. 14, no. 1, Jan. 2005, pp. 155–69. EBSCOhost, https://doi.org/10.1093/hmg/ddi017.

APA

Arimura, T., Helbling-Leclerc, A., Massart, C., Varnous, S., Niel, F., Lacène, E., Fromes, Y., Toussaint, M., Mura, A.-M., Keller, D. I., Amthor, H., Isnard, R., Malissen, M., Schwartz, K., & Bonne, G. (2005). Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies. Human Molecular Genetics, 14(1), 155–169. https://doi.org/10.1093/hmg/ddi017

Chicago

Arimura, Takuro, Anne Helbling-Leclerc, Catherine Massart, Shaida Varnous, Florence Niel, Emmanuelle Lacène, Yves Fromes, et al. 2005. “Mouse Model Carrying H222P-Lmna Mutation Develops Muscular Dystrophy and Dilated Cardiomyopathy Similar to Human Striated Muscle Laminopathies.” Human Molecular Genetics 14 (1): 155–69. doi:10.1093/hmg/ddi017.