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CRISPR/Cas9 Gene Editing of Hematopoietic Stem and Progenitor Cells for Gene Therapy Applications
Published on: August 9, 2022
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CRISPR-Cas9 Gene Editing for Sickle Cell Disease and β-Thalassemia. Reply
Haydar Frangoul1, Tony W Ho2, Selim Corbacioglu3
1Sarah Cannon Center for Blood Cancer at the Children's Hospital at TriStar Centennial, Nashville, TN haydar.frangoul@hcahealthcare.com.
The New England Journal of Medicine
|June 9, 2021
Abstract
No abstract available in PubMed .
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