Cita APA

Kocoglu, C., Gundogdu, A., Kocaman, G., Kahraman-Koytak, P., Uluc, K., Kiziltan, G., . . . Basak, A. N. (2018). Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families. Neurol Genet.

Chicago Style Citation

Kocoglu, Cemile, et al. "Homozygous CAPN1 Mutations Causing a Spastic-ataxia Phenotype in 2 Families." Neurol Genet 2018.

Cita MLA

Kocoglu, Cemile, et al. "Homozygous CAPN1 Mutations Causing a Spastic-ataxia Phenotype in 2 Families." Neurol Genet 2018.