Cita APA

Seidahmed, M. Z., Hamad, M. H., AlBakheet, A., Elmalik, S. A., AlDrees, A., Al-Sufayan, J., . . . Kaya, N. (2020). Ancient founder mutation in RUBCN: A second unrelated family confirms Salih ataxia (SCAR15). BMC Neurol.

Chicago Style Citation

Seidahmed, Mohammed Z., et al. "Ancient Founder Mutation in RUBCN: A Second Unrelated Family Confirms Salih Ataxia (SCAR15)." BMC Neurol 2020.

Cita MLA

Seidahmed, Mohammed Z., et al. "Ancient Founder Mutation in RUBCN: A Second Unrelated Family Confirms Salih Ataxia (SCAR15)." BMC Neurol 2020.