Nicholls, K.; Wise, A.; Elliot, D.; ter Huurne, M.; Fuller, M.; Ricardo, S.
Mutation-Specific Cardiomyocyte Lines from Patients with Fabry Disease: A Sustainable In Vitro Model to Investigate Structure, Function, and Disease Mechanisms. Int. J. Transl. Med. 2025, 5, 15.
https://doi.org/10.3390/ijtm5020015
AMA Style
Nicholls K, Wise A, Elliot D, ter Huurne M, Fuller M, Ricardo S.
Mutation-Specific Cardiomyocyte Lines from Patients with Fabry Disease: A Sustainable In Vitro Model to Investigate Structure, Function, and Disease Mechanisms. International Journal of Translational Medicine. 2025; 5(2):15.
https://doi.org/10.3390/ijtm5020015
Chicago/Turabian Style
Nicholls, Kathleen, Andrea Wise, David Elliot, Menno ter Huurne, Maria Fuller, and Sharon Ricardo.
2025. "Mutation-Specific Cardiomyocyte Lines from Patients with Fabry Disease: A Sustainable In Vitro Model to Investigate Structure, Function, and Disease Mechanisms" International Journal of Translational Medicine 5, no. 2: 15.
https://doi.org/10.3390/ijtm5020015
APA Style
Nicholls, K., Wise, A., Elliot, D., ter Huurne, M., Fuller, M., & Ricardo, S.
(2025). Mutation-Specific Cardiomyocyte Lines from Patients with Fabry Disease: A Sustainable In Vitro Model to Investigate Structure, Function, and Disease Mechanisms. International Journal of Translational Medicine, 5(2), 15.
https://doi.org/10.3390/ijtm5020015