Cita APA

Kabir, F., Ullah, I., Ali, S., Gottsch, A. D., Naeem, M. A., Assir, M. Z., . . . Riazuddin, S. A. (2016). Loss of function mutations in RP1 are responsible for retinitis pigmentosa in consanguineous familial cases. Mol Vis.

Chicago Style Citation

Kabir, Firoz, et al. "Loss of Function Mutations in RP1 Are Responsible for Retinitis Pigmentosa in Consanguineous Familial Cases." Mol Vis 2016.

Cita MLA

Kabir, Firoz, et al. "Loss of Function Mutations in RP1 Are Responsible for Retinitis Pigmentosa in Consanguineous Familial Cases." Mol Vis 2016.