Cite
HARVARD Citation
Cai, L. et al. (2018). A Universal Approach to Correct Various HBB Gene Mutations in Human Stem Cells for Gene Therapy of Beta‐Thalassemia and Sickle Cell Disease. Stem cells translational medicine. pp. 87-97. [Online].
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Cai, L. et al. (2018). A Universal Approach to Correct Various HBB Gene Mutations in Human Stem Cells for Gene Therapy of Beta‐Thalassemia and Sickle Cell Disease. Stem cells translational medicine. pp. 87-97. [Online].