APA (7th ed.) Citation

M, B., M, K., P, H., & Y, F. (2013). Partial protoporphyrinogen oxidase (PPOX) gene deletions, due to different Alu-mediated mechanisms, identified by MLPA analysis in patients with variegate porphyria. Orphanet journal of rare diseases, 8, 13. https://doi.org/10.1186/1750-1172-8-13

Chicago Style (17th ed.) Citation

M, Barbaro, Kotajärvi M, Harper P, and Floderus Y. "Partial Protoporphyrinogen Oxidase (PPOX) Gene Deletions, Due to Different Alu-mediated Mechanisms, Identified by MLPA Analysis in Patients with Variegate Porphyria." Orphanet Journal of Rare Diseases 8 (2013): 13. https://doi.org/10.1186/1750-1172-8-13.

MLA (9th ed.) Citation

M, Barbaro, et al. "Partial Protoporphyrinogen Oxidase (PPOX) Gene Deletions, Due to Different Alu-mediated Mechanisms, Identified by MLPA Analysis in Patients with Variegate Porphyria." Orphanet Journal of Rare Diseases, vol. 8, 2013, p. 13, https://doi.org/10.1186/1750-1172-8-13.