APA (7th ed.) Citation

EE, B., CI, W., K, S., RM, B., K, G., NL, T., . . . NH, M. (2014). Exome sequencing identifies a rare HSPG2 variant associated with familial idiopathic scoliosis. G3 (Bethesda, Md.), 5(2), 167. https://doi.org/10.1534/g3.114.015669

Chicago Style (17th ed.) Citation

EE, Baschal, et al. "Exome Sequencing Identifies a Rare HSPG2 Variant Associated with Familial Idiopathic Scoliosis." G3 (Bethesda, Md.) 5, no. 2 (2014): 167. https://doi.org/10.1534/g3.114.015669.

MLA (9th ed.) Citation

EE, Baschal, et al. "Exome Sequencing Identifies a Rare HSPG2 Variant Associated with Familial Idiopathic Scoliosis." G3 (Bethesda, Md.), vol. 5, no. 2, 2014, p. 167, https://doi.org/10.1534/g3.114.015669.