Cite
Rett syndrome – biological pathways leading from MECP2 to disorder phenotypes
MLA
Friederike Ehrhart, et al. “Rett Syndrome – Biological Pathways Leading from MECP2 to Disorder Phenotypes.” Orphanet Journal of Rare Diseases, vol. 11, no. 1, Nov. 2016, pp. 1–13. EBSCOhost, https://doi.org/10.1186/s13023-016-0545-5.
APA
Friederike Ehrhart, Susan L. M. Coort, Elisa Cirillo, Eric Smeets, Chris T. Evelo, & Leopold M. G. Curfs. (2016). Rett syndrome – biological pathways leading from MECP2 to disorder phenotypes. Orphanet Journal of Rare Diseases, 11(1), 1–13. https://doi.org/10.1186/s13023-016-0545-5
Chicago
Friederike Ehrhart, Susan L. M. Coort, Elisa Cirillo, Eric Smeets, Chris T. Evelo, and Leopold M. G. Curfs. 2016. “Rett Syndrome – Biological Pathways Leading from MECP2 to Disorder Phenotypes.” Orphanet Journal of Rare Diseases 11 (1): 1–13. doi:10.1186/s13023-016-0545-5.