Mitochondrial Membrane Protein-Associated Neurodegeneration (MPAN): Two Phenotypes--Dystonia and Spastic Paraparesis.

MLA

Kola, Sruthi, et al. “Mitochondrial Membrane Protein-Associated Neurodegeneration (MPAN): Two Phenotypes--Dystonia and Spastic Paraparesis.” Annals of Indian Academy of Neurology, vol. 25, no. 6, Nov. 2022, pp. 1200–02. EBSCOhost, https://doi.org/10.4103/aian.aian_658_22.

APA

Kola, S., Meka, S. S. L., Fathima, S. T., Wahed, A., Kandadai, R. M., & Borgohain, R. (2022). Mitochondrial Membrane Protein-Associated Neurodegeneration (MPAN): Two Phenotypes--Dystonia and Spastic Paraparesis. Annals of Indian Academy of Neurology, 25(6), 1200–1202. https://doi.org/10.4103/aian.aian_658_22

Chicago

Kola, Sruthi, Sai S. L. Meka, Syed T. Fathima, Abdul Wahed, Rukmini M. Kandadai, and Rupam Borgohain. 2022. “Mitochondrial Membrane Protein-Associated Neurodegeneration (MPAN): Two Phenotypes--Dystonia and Spastic Paraparesis.” Annals of Indian Academy of Neurology 25 (6): 1200–1202. doi:10.4103/aian.aian_658_22.