S, C., DA, P., MA, L., MM, P., MC, B., FM, G., . . . HV, A. (2025). From Severe Neonatal Encephalopathy to Slowly Neurologic Progressive Disease: Pyruvate Dehydrogenase Deficiency Related to PDHA1 Variants. Journal of child neurology, 8830738251404115. https://doi.org/10.1177/08830738251404115
Chicago Style (17th ed.) CitationS, Corbaz, et al. "From Severe Neonatal Encephalopathy to Slowly Neurologic Progressive Disease: Pyruvate Dehydrogenase Deficiency Related to PDHA1 Variants." Journal of Child Neurology 2025: 8830738251404115. https://doi.org/10.1177/08830738251404115.
MLA (9th ed.) CitationS, Corbaz, et al. "From Severe Neonatal Encephalopathy to Slowly Neurologic Progressive Disease: Pyruvate Dehydrogenase Deficiency Related to PDHA1 Variants." Journal of Child Neurology, 2025, p. 8830738251404115, https://doi.org/10.1177/08830738251404115.