APA সাইটেশন

Ye, L., Wang, J., Tan, Y., Beyer, A. I., Xie, F., Muench, M. O., & Kan, Y. W. (2016). Genome editing using CRISPR-Cas9 to create the HPFH genotype in HSPCs: An approach for treating sickle cell disease and β-thalassemia. Proc Natl Acad Sci U S A.

শিকাগো স্টাইলে সাইটেশন

Ye, Lin, Jiaming Wang, Yuting Tan, Ashley I. Beyer, Fei Xie, Marcus O. Muench, এবং Yuet Wai Kan. "Genome Editing Using CRISPR-Cas9 to Create the HPFH Genotype in HSPCs: An Approach for Treating Sickle Cell Disease and β-thalassemia." Proc Natl Acad Sci U S A 2016.

এমএলএ সাইটেশন

Ye, Lin, et al. "Genome Editing Using CRISPR-Cas9 to Create the HPFH Genotype in HSPCs: An Approach for Treating Sickle Cell Disease and β-thalassemia." Proc Natl Acad Sci U S A 2016.