Cite
Lack of mitochondrial complex I assembly factor NDUFAF2 results in a distinctive infantile-onset brainstem neurodegenerative disease with early lethality.
MLA
Abu Hanna, Firas, et al. “Lack of Mitochondrial Complex I Assembly Factor NDUFAF2 Results in a Distinctive Infantile-Onset Brainstem Neurodegenerative Disease with Early Lethality.” Orphanet Journal of Rare Diseases, vol. 19, no. 1, Feb. 2024, pp. 1–11. EBSCOhost, https://doi.org/10.1186/s13023-024-03094-0.
APA
Abu Hanna, F., Zehavi, Y., Cohen-Barak, E., Khayat, M., Warwar, N., Shreter, R., Rodenburg, R. J., & Spiegel, R. (2024). Lack of mitochondrial complex I assembly factor NDUFAF2 results in a distinctive infantile-onset brainstem neurodegenerative disease with early lethality. Orphanet Journal of Rare Diseases, 19(1), 1–11. https://doi.org/10.1186/s13023-024-03094-0
Chicago
Abu Hanna, Firas, Yoav Zehavi, Eran Cohen-Barak, Morad Khayat, Nasim Warwar, Roni Shreter, Richard J. Rodenburg, and Ronen Spiegel. 2024. “Lack of Mitochondrial Complex I Assembly Factor NDUFAF2 Results in a Distinctive Infantile-Onset Brainstem Neurodegenerative Disease with Early Lethality.” Orphanet Journal of Rare Diseases 19 (1): 1–11. doi:10.1186/s13023-024-03094-0.