Cita APA

Chelban, V., Patel, N., Vandrovcova, J., Zanetti, M. N., Lynch, D. S., Ryten, M., . . . Houlden, H. (2017). Mutations in NKX6-2 Cause Progressive Spastic Ataxia and Hypomyelination. Web

Citación estilo Chicago

Chelban, Viorica, et al. Mutations in NKX6-2 Cause Progressive Spastic Ataxia and Hypomyelination. 2017.

Cita MLA

Chelban, Viorica, et al. Mutations in NKX6-2 Cause Progressive Spastic Ataxia and Hypomyelination. 2017.