APA aipamena

Hedberg-Oldfors, C., Darin, N., Thomsen, C., Lindberg, C., & Oldfors, A. (2020). COX deficiency and leukoencephalopathy due to a novel homozygous APOPT1/COA8 mutation. Neurol Genet.

Chicago Style aipamena

Hedberg-Oldfors, Carola, Niklas Darin, Christer Thomsen, Christopher Lindberg, and Anders Oldfors. "COX Deficiency and Leukoencephalopathy Due to a Novel Homozygous APOPT1/COA8 Mutation." Neurol Genet 2020.

MLA aipamena

Hedberg-Oldfors, Carola, et al. "COX Deficiency and Leukoencephalopathy Due to a Novel Homozygous APOPT1/COA8 Mutation." Neurol Genet 2020.