APA aipamena

Bouwkamp, C. G., Afawi, Z., Fattal-Valevski, A., Krabbendam, I. E., Rivetti, S., Masalha, R., . . . Kushner, S. A. (2018). ACO2 homozygous missense mutation associated with complicated hereditary spastic paraplegia. Neurol Genet.

Chicago Style aipamena

Bouwkamp, Christian G., et al. "ACO2 Homozygous Missense Mutation Associated With Complicated Hereditary Spastic Paraplegia." Neurol Genet 2018.

MLA aipamena

Bouwkamp, Christian G., et al. "ACO2 Homozygous Missense Mutation Associated With Complicated Hereditary Spastic Paraplegia." Neurol Genet 2018.