Diagnostic Challenges in Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency: Clinical, Morphological, and Genetic Aspects.

MLA

Lupica, Antonino, et al. “Diagnostic Challenges in Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency: Clinical, Morphological, and Genetic Aspects.” Frontiers in Neurology, vol. 13, Mar. 2022, p. 815523. EBSCOhost, https://doi.org/10.3389/fneur.2022.815523.

APA

Lupica, A., Oteri, R., Volta, S., Ghezzi, D., Drago, S. F. A., Rodolico, C., Musumeci, O., & Toscano, A. (2022). Diagnostic Challenges in Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency: Clinical, Morphological, and Genetic Aspects. Frontiers in Neurology, 13, 815523. https://doi.org/10.3389/fneur.2022.815523

Chicago

Lupica, Antonino, Rosaria Oteri, Sara Volta, Daniele Ghezzi, Selene Francesca Anna Drago, Carmelo Rodolico, Olimpia Musumeci, and Antonio Toscano. 2022. “Diagnostic Challenges in Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency: Clinical, Morphological, and Genetic Aspects.” Frontiers in Neurology 13 (March): 815523. doi:10.3389/fneur.2022.815523.