Stepien, K.M.; Cufflin, N.; Donald, A.; Jones, S.; Church, H.; Hargreaves, I.P.
Secondary Mitochondrial Dysfunction as a Cause of Neurodegenerative Dysfunction in Lysosomal Storage Diseases and an Overview of Potential Therapies. Int. J. Mol. Sci. 2022, 23, 10573.
https://doi.org/10.3390/ijms231810573
AMA Style
Stepien KM, Cufflin N, Donald A, Jones S, Church H, Hargreaves IP.
Secondary Mitochondrial Dysfunction as a Cause of Neurodegenerative Dysfunction in Lysosomal Storage Diseases and an Overview of Potential Therapies. International Journal of Molecular Sciences. 2022; 23(18):10573.
https://doi.org/10.3390/ijms231810573
Chicago/Turabian Style
Stepien, Karolina M., Neve Cufflin, Aimee Donald, Simon Jones, Heather Church, and Iain P. Hargreaves.
2022. "Secondary Mitochondrial Dysfunction as a Cause of Neurodegenerative Dysfunction in Lysosomal Storage Diseases and an Overview of Potential Therapies" International Journal of Molecular Sciences 23, no. 18: 10573.
https://doi.org/10.3390/ijms231810573
APA Style
Stepien, K. M., Cufflin, N., Donald, A., Jones, S., Church, H., & Hargreaves, I. P.
(2022). Secondary Mitochondrial Dysfunction as a Cause of Neurodegenerative Dysfunction in Lysosomal Storage Diseases and an Overview of Potential Therapies. International Journal of Molecular Sciences, 23(18), 10573.
https://doi.org/10.3390/ijms231810573