A fatal case of neonatal onset multiple acyl-CoA dehydrogenase deficiency caused by novel mutation of ETFDH gene: case report.

MLA

De Pasquale, Loredana, et al. “A Fatal Case of Neonatal Onset Multiple Acyl-CoA Dehydrogenase Deficiency Caused by Novel Mutation of ETFDH Gene: Case Report.” Italian Journal of Pediatrics, vol. 48, no. 1, Sept. 2022, p. 164. EBSCOhost, https://doi.org/10.1186/s13052-022-01356-w.

APA

De Pasquale, L., Meo, P., Fulia, F., Anania, A., Meli, V., Mondello, A., Raimondo, M. T., Tulino, V., Coletta, M. S., & Cacace, C. (2022). A fatal case of neonatal onset multiple acyl-CoA dehydrogenase deficiency caused by novel mutation of ETFDH gene: case report. Italian Journal of Pediatrics, 48(1), 164. https://doi.org/10.1186/s13052-022-01356-w

Chicago

De Pasquale, Loredana, Petronilla Meo, Francesco Fulia, Antonio Anania, Valerio Meli, Antonina Mondello, Maria Tindara Raimondo, Viviana Tulino, Maria Sole Coletta, and Caterina Cacace. 2022. “A Fatal Case of Neonatal Onset Multiple Acyl-CoA Dehydrogenase Deficiency Caused by Novel Mutation of ETFDH Gene: Case Report.” Italian Journal of Pediatrics 48 (1): 164. doi:10.1186/s13052-022-01356-w.