APA ציטוט

Jun, I., Ji, Y. W., Choi, S., Lee, B. R., Min, J. S., & Kim, E. K. (2021). Compound heterozygous mutations in TGFBI cause a severe phenotype of granular corneal dystrophy type 2. Sci Rep.

Citação norma Chicago

Jun, Ikhyun, Yong Woo Ji, Seung-il Choi, Bo Ram Lee, Ji Sang Min, and Eung Kweon Kim. "Compound Heterozygous Mutations in TGFBI Cause a Severe Phenotype of Granular Corneal Dystrophy Type 2." Sci Rep 2021.

ציטוט MLA

Jun, Ikhyun, et al. "Compound Heterozygous Mutations in TGFBI Cause a Severe Phenotype of Granular Corneal Dystrophy Type 2." Sci Rep 2021.