Dyfyniad APA

Chelban, V., Alsagob, M., Kloth, K., Chirita‐Emandi, A., Vandrovcova, J., Maroofian, R., . . . Kaya, N. (2019). Genetic and phenotypic characterization of NKX6‐2‐related spastic ataxia and hypomyelination. Eur J Neurol.

Dyfyniad Arddull Chicago

Chelban, V., et al. "Genetic and Phenotypic Characterization of NKX6‐2‐related Spastic Ataxia and Hypomyelination." Eur J Neurol 2019.

Dyfyniad MLA

Chelban, V., et al. "Genetic and Phenotypic Characterization of NKX6‐2‐related Spastic Ataxia and Hypomyelination." Eur J Neurol 2019.

Rhybudd: Mae'n bosib nad yw'r dyfyniadau hyn bob amser yn 100% cywir.