Cita APA

Xiao, X., Sun, W., Ouyang, J., Li, S., Jia, X., Tan, Z., . . . Zhang, Q. (2019). Novel truncation mutations in MYRF cause autosomal dominant high hyperopia mapped to 11p12–q13.3. Hum Genet.

Chicago Style Citation

Xiao, Xueshan, Wenmin Sun, Jiamin Ouyang, Shiqiang Li, Xiaoyun Jia, Zhiqun Tan, J. Fielding Hejtmancik, i Qingjiong Zhang. "Novel Truncation Mutations in MYRF Cause Autosomal Dominant High Hyperopia Mapped to 11p12–q13.3." Hum Genet 2019.

Cita MLA

Xiao, Xueshan, et al. "Novel Truncation Mutations in MYRF Cause Autosomal Dominant High Hyperopia Mapped to 11p12–q13.3." Hum Genet 2019.