Cita APA

Gan, P., Baicu, C., Watanabe, H., Wang, K., Tao, G., Judge, D. P., . . . Sucov, H. M. (2020). The prevalent I686T human variant and loss-of-function mutations in the cardiomyocyte-specific kinase gene TNNI3K cause adverse contractility and concentric remodeling in mice. Hum Mol Genet.

Chicago Style Citation

Gan, Peiheng, et al. "The Prevalent I686T Human Variant and Loss-of-function Mutations in the Cardiomyocyte-specific Kinase Gene TNNI3K Cause Adverse Contractility and Concentric Remodeling in Mice." Hum Mol Genet 2020.

Cita MLA

Gan, Peiheng, et al. "The Prevalent I686T Human Variant and Loss-of-function Mutations in the Cardiomyocyte-specific Kinase Gene TNNI3K Cause Adverse Contractility and Concentric Remodeling in Mice." Hum Mol Genet 2020.