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Scope
The section Genome Editing in Blood Disorders provides a platform for publishing the technological development and application of genome editing in blood diseases.
Scope
Gene Editing for the treatment of inherited and acquired blood disorders is a promising new approach which has the potential to provide lifelong correction of many debilitating diseases.
This section of Frontiers in Genome Editing is focused on providing a platform for the publication of improvements in existing gene editing methods and for initial publication of novel gene editing methods for the treatment of blood disorders. Review articles will also be published; these reviews will play an important role in integrating the field, providing novel perspectives, and serving as educational materials for graduate and professional students, basic and physician scientists and physicians practicing in large and small communities world-wide.
A small sample of blood disorders, for which gene editing strategies will be published, include:
• Alpha- and beta-thalassemia
• Severe combined immune deficiency
• Autoimmunity
• HIV/AIDS
• CAR-T cell therapy for leukemias and solid tumors.
The ultimate goal is to provide a forum for the publication of gene editing approaches for blood disorders as these methods progress from basic science to clinical medicine.
Indexed in: CLOCKSS, CrossRef, DOAJ, Google Scholar, OpenAIRE, PubMed Central (PMC)
PMCID: NA
Genome Editing in Blood Disorders welcomes submissions of the following article types: Brief Research Report, Correction, Editorial, General Commentary, Hypothesis and Theory, Methods, Mini Review, Opinion, Original Research, Perspective and Review.
All manuscripts must be submitted directly to the section Genome Editing in Blood Disorders, where they are peer-reviewed by the Associate and Review Editors of the specialty section.
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