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Gene and Cell Therapy for β-Thalassemia and Sickle Cell Disease with Induced Pluripotent Stem Cells (iPSCs): The Next Frontier. https://t.co/WSkjurxBxZ https://t.co/fuXHrXeWDI
Gene and Cell Therapies for Beta-Globinopathies
Overview of attention for book
Table of Contents
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Altmetric BadgeBook Overview
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Altmetric BadgeChapter 1 Clinical Features of β-Thalassemia and Sickle Cell Disease
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Altmetric BadgeChapter 2 Genetic Basis and Genetic Modifiers of β-Thalassemia and Sickle Cell Disease
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Altmetric BadgeChapter 3 Current Standards of Care and Long Term Outcomes for Thalassemia and Sickle Cell Disease
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Altmetric BadgeChapter 4 Allogeneic/Matched Related Transplantation for β-Thalassemia and Sickle Cell Anemia
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Altmetric BadgeChapter 5 Alternative Donor/Unrelated Donor Transplants for the β-Thalassemia and Sickle Cell Disease
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Altmetric BadgeChapter 6 Gene Addition Strategies for β-Thalassemia and Sickle Cell Anemia
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Altmetric BadgeChapter 7 Reactivation of Fetal Hemoglobin for Treating β-Thalassemia and Sickle Cell Disease
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Altmetric BadgeChapter 8 Genome Editing for the β-Hemoglobinopathies
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Altmetric BadgeChapter 9 Gene and Cell Therapy for β-Thalassemia and Sickle Cell Disease with Induced Pluripotent Stem Cells (iPSCs): The Next Frontier
Attention for Chapter 9:
Gene and Cell Therapy for β-Thalassemia and Sickle Cell Disease with Induced Pluripotent Stem Cells (iPSCs): The Next Frontier