APA (7th ed.) Citation

Torraco, A., Bianchi, M., Verrigni, D., Gelmetti, V., Riley, L., Niceta, M., . . . Christodoulou, J. (2017). A novel mutation in NDUFB11 unveils a new clinical phenotype associated with lactic acidosis and sideroblastic anemia. Clinical Genetics, 91(3), 441. https://doi.org/10.1111/cge.12790

Chicago Style (17th ed.) Citation

Torraco, A., et al. "A Novel Mutation in NDUFB11 Unveils a New Clinical Phenotype Associated with Lactic Acidosis and Sideroblastic Anemia." Clinical Genetics 91, no. 3 (2017): 441. https://doi.org/10.1111/cge.12790.

MLA (9th ed.) Citation

Torraco, A., et al. "A Novel Mutation in NDUFB11 Unveils a New Clinical Phenotype Associated with Lactic Acidosis and Sideroblastic Anemia." Clinical Genetics, vol. 91, no. 3, 2017, p. 441, https://doi.org/10.1111/cge.12790.