Chapter 1 Clinical Features of β-Thalassemia and Sickle Cell Disease

Chapter 2 Genetic Basis and Genetic Modifiers of β-Thalassemia and Sickle Cell Disease

Chapter 3 Current Standards of Care and Long Term Outcomes for Thalassemia and Sickle Cell Disease

Chapter 4 Allogeneic/Matched Related Transplantation for β-Thalassemia and Sickle Cell Anemia

Chapter 5 Alternative Donor/Unrelated Donor Transplants for the β-Thalassemia and Sickle Cell Disease

Chapter 7 Reactivation of Fetal Hemoglobin for Treating β-Thalassemia and Sickle Cell Disease

Chapter 8 Genome Editing for the β-Hemoglobinopathies

Chapter 9 Gene and Cell Therapy for β-Thalassemia and Sickle Cell Disease with Induced Pluripotent Stem Cells (iPSCs): The Next Frontier