APA (7th ed.) Citation

Bujakowska, K. M., Zhang, Q., Siemiatkowska, A. M., Liu, Q., Place, E., Falk, M. J., . . . Pierce, E. A. (2015). Mutations in IFT172 cause isolated retinal degeneration and Bardet–Biedl syndrome. Human molecular genetics, 24(1), 230-242. https://doi.org/10.1093/hmg/ddu441

Chicago Style (17th ed.) Citation

Bujakowska, Kinga M., et al. "Mutations in IFT172 Cause Isolated Retinal Degeneration and Bardet–Biedl Syndrome." Human Molecular Genetics 24, no. 1 (2015): 230-242. https://doi.org/10.1093/hmg/ddu441.

MLA (9th ed.) Citation

Bujakowska, Kinga M., et al. "Mutations in IFT172 Cause Isolated Retinal Degeneration and Bardet–Biedl Syndrome." Human Molecular Genetics, vol. 24, no. 1, 2015, pp. 230-242, https://doi.org/10.1093/hmg/ddu441.