Cite
A Barth Syndrome Patient-Derived D75H Point Mutation in TAFAZZIN Drives Progressive Cardiomyopathy in Mice
MLA
Paige L. Snider, et al. “A Barth Syndrome Patient-Derived D75H Point Mutation in TAFAZZIN Drives Progressive Cardiomyopathy in Mice.” International Journal of Molecular Sciences, vol. 25, no. 15, July 2024, p. 8201. EBSCOhost, https://doi.org/10.3390/ijms25158201.
APA
Paige L. Snider, Elizabeth A. Sierra Potchanant, Zejin Sun, Donna M. Edwards, Ka-Kui Chan, Catalina Matias, Junya Awata, Aditya Sheth, P. Melanie Pride, R. Mark Payne, Michael Rubart, Jeffrey J. Brault, Michael T. Chin, Grzegorz Nalepa, & Simon J. Conway. (2024). A Barth Syndrome Patient-Derived D75H Point Mutation in TAFAZZIN Drives Progressive Cardiomyopathy in Mice. International Journal of Molecular Sciences, 25(15), 8201. https://doi.org/10.3390/ijms25158201
Chicago
Paige L. Snider, Elizabeth A. Sierra Potchanant, Zejin Sun, Donna M. Edwards, Ka-Kui Chan, Catalina Matias, Junya Awata, et al. 2024. “A Barth Syndrome Patient-Derived D75H Point Mutation in TAFAZZIN Drives Progressive Cardiomyopathy in Mice.” International Journal of Molecular Sciences 25 (15): 8201. doi:10.3390/ijms25158201.