Fetal hemoglobin in β hemoglobinopathies: Is enough too much?
Author:
Affiliation:
1. Department of Medicine, Division of Hematology and Medical Oncology Boston University School of Medicine Boston Massachusetts 02118 USA
Publisher
Wiley
Subject
Hematology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajh.26518
Reference30 articles.
1. Biologic and Clinical Efficacy of LentiGlobin for Sickle Cell Disease
2. CRISPR-Cas9 Gene Editing for Sickle Cell Disease and β-Thalassemia
3. Post-Transcriptional Genetic Silencing ofBCL11Ato Treat Sickle Cell Disease
4. Molecular medicine: found in translation;Orkin SH;Med (NY),2021
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1. Adenine base editor–mediated correction of the common and severe IVS1-110 (G>A) β-thalassemia mutation;Blood;2023-03-09
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