APA (7th ed.) Citation

Luscieti, S., Tolle, G., Aranda, J., Campos, C. B., Risse, F., Morán, E., . . . Sánchez, M. (2013). Novel mutations in the ferritin-L iron-responsive element that only mildly impair IRP binding cause hereditary hyperferritinaemia cataract syndrome. Orphanet journal of rare diseases, 8, . https://doi.org/10.1186/1750-1172-8-30

Chicago Style (17th ed.) Citation

Luscieti, Sara, Gabriele Tolle, Jessica Aranda, Carmen Benet Campos, Frank Risse, Érica Morán, Martina Muckenthaler, and Mayka Sánchez. "Novel Mutations in the Ferritin-L Iron-responsive Element That Only Mildly Impair IRP Binding Cause Hereditary Hyperferritinaemia Cataract Syndrome." Orphanet Journal of Rare Diseases 8 (2013). https://doi.org/10.1186/1750-1172-8-30.

MLA (9th ed.) Citation

Luscieti, Sara, et al. "Novel Mutations in the Ferritin-L Iron-responsive Element That Only Mildly Impair IRP Binding Cause Hereditary Hyperferritinaemia Cataract Syndrome." Orphanet Journal of Rare Diseases, vol. 8, 2013, https://doi.org/10.1186/1750-1172-8-30.