APA (7th ed.) Citation

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 neurology, 20(1), 207-7. https://doi.org/10.1186/s12883-020-01761-w

Chicago Style (17th ed.) Citation

Seidahmed, Mohammed Z., et al. "Ancient Founder Mutation in RUBCN: A Second Unrelated Family Confirms Salih Ataxia (SCAR15)." BMC Neurology 20, no. 1 (2020): 207-7. https://doi.org/10.1186/s12883-020-01761-w.

MLA (9th ed.) Citation

Seidahmed, Mohammed Z., et al. "Ancient Founder Mutation in RUBCN: A Second Unrelated Family Confirms Salih Ataxia (SCAR15)." BMC Neurology, vol. 20, no. 1, 2020, pp. 207-7, https://doi.org/10.1186/s12883-020-01761-w.