Infantile onset carnitine palmitoyltransferase 2 deficiency: Cortical polymicrogyria, schizencephaly, and gray matter heterotopias in an adolescent with normal development.

MLA

Shelihan, Ivan, et al. “Infantile Onset Carnitine Palmitoyltransferase 2 Deficiency: Cortical Polymicrogyria, Schizencephaly, and Gray Matter Heterotopias in an Adolescent with Normal Development.” JIMD Reports, vol. 63, no. 1, Sept. 2021, pp. 3–10. EBSCOhost, https://doi.org/10.1002/jmd2.12243.

APA

Shelihan, I., Rossignol, E., Décarie, J.-C., Bonnefont, J.-P., Brivet, M., Brunel-Guitton, C., & Mitchell, G. A. (2021). Infantile onset carnitine palmitoyltransferase 2 deficiency: Cortical polymicrogyria, schizencephaly, and gray matter heterotopias in an adolescent with normal development. JIMD Reports, 63(1), 3–10. https://doi.org/10.1002/jmd2.12243

Chicago

Shelihan, Ivan, Elsa Rossignol, Jean-Claude Décarie, Jean-Paul Bonnefont, Michèle Brivet, Catherine Brunel-Guitton, and Grant A Mitchell. 2021. “Infantile Onset Carnitine Palmitoyltransferase 2 Deficiency: Cortical Polymicrogyria, Schizencephaly, and Gray Matter Heterotopias in an Adolescent with Normal Development.” JIMD Reports 63 (1): 3–10. doi:10.1002/jmd2.12243.