APA (7th ed.) Citation

Bailey, L., Ambruso, D., Grabowski, G., & Burrow, T. A. (2015). Combination therapy (eliglustat + velaglucerase alfa) in a pediatric patient with Gaucher disease type 1 and hereditary spherocytosis. Molecular Genetics & Metabolism, 114(2), S17. https://doi.org/10.1016/j.ymgme.2014.12.020

Chicago Style (17th ed.) Citation

Bailey, Laurie, Daniel Ambruso, Gregory Grabowski, and Thomas A. Burrow. "Combination Therapy (eliglustat + Velaglucerase Alfa) in a Pediatric Patient with Gaucher Disease Type 1 and Hereditary Spherocytosis." Molecular Genetics & Metabolism 114, no. 2 (2015): S17. https://doi.org/10.1016/j.ymgme.2014.12.020.

MLA (9th ed.) Citation

Bailey, Laurie, et al. "Combination Therapy (eliglustat + Velaglucerase Alfa) in a Pediatric Patient with Gaucher Disease Type 1 and Hereditary Spherocytosis." Molecular Genetics & Metabolism, vol. 114, no. 2, 2015, p. S17, https://doi.org/10.1016/j.ymgme.2014.12.020.