APA (7th ed.) Citation

Munns, C., Fahiminiya, S., Poudel, N., Munteanu, M., Majewski, J., Sillence, D., . . . Hinsdale, M. (2015). Homozygosity for Frameshift Mutations in XYLT2 Result in a Spondylo-Ocular Syndrome with Bone Fragility, Cataracts, and Hearing Defects. American journal of human genetics, 96(6), 971-978. https://doi.org/10.1016/j.ajhg.2015.04.017

Chicago Style (17th ed.) Citation

Munns, Craig F, et al. "Homozygosity for Frameshift Mutations in XYLT2 Result in a Spondylo-Ocular Syndrome with Bone Fragility, Cataracts, and Hearing Defects." American Journal of Human Genetics 96, no. 6 (2015): 971-978. https://doi.org/10.1016/j.ajhg.2015.04.017.

MLA (9th ed.) Citation

Munns, Craig F, et al. "Homozygosity for Frameshift Mutations in XYLT2 Result in a Spondylo-Ocular Syndrome with Bone Fragility, Cataracts, and Hearing Defects." American Journal of Human Genetics, vol. 96, no. 6, 2015, pp. 971-978, https://doi.org/10.1016/j.ajhg.2015.04.017.