Ali, S. R., Bryce, J., Tan, L. E., Hiort, O., Pereira, A. M., van den Akker, E. L. T., . . . Ahmed, S. F. (2020). The EuRRECa Project as a Model for Data Access and Governance Policies for Rare Disease Registries That Collect Clinical Outcomes. Int J Environ Res Public Health.

Ali, Salma R., et al. "The EuRRECa Project As a Model for Data Access and Governance Policies for Rare Disease Registries That Collect Clinical Outcomes." Int J Environ Res Public Health 2020.

Ali, Salma R., et al. "The EuRRECa Project As a Model for Data Access and Governance Policies for Rare Disease Registries That Collect Clinical Outcomes." Int J Environ Res Public Health 2020.