APA (7th ed.) Citation

M, R., HL, S., LF, P., EM, B., C, B., A, J., . . . C, G. (2013). ZNF469 frequently mutated in the brittle cornea syndrome (BCS) is a single exon gene possibly regulating the expression of several extracellular matrix components. Molecular genetics and metabolism, 109(3), 289. https://doi.org/10.1016/j.ymgme.2013.04.014

Chicago Style (17th ed.) Citation

M, Rohrbach, et al. "ZNF469 Frequently Mutated in the Brittle Cornea Syndrome (BCS) Is a Single Exon Gene Possibly Regulating the Expression of Several Extracellular Matrix Components." Molecular Genetics and Metabolism 109, no. 3 (2013): 289. https://doi.org/10.1016/j.ymgme.2013.04.014.

MLA (9th ed.) Citation

M, Rohrbach, et al. "ZNF469 Frequently Mutated in the Brittle Cornea Syndrome (BCS) Is a Single Exon Gene Possibly Regulating the Expression of Several Extracellular Matrix Components." Molecular Genetics and Metabolism, vol. 109, no. 3, 2013, p. 289, https://doi.org/10.1016/j.ymgme.2013.04.014.