Editorial: Genome Editing to Treat Cystic Fibrosis and Other Pulmonary Diseases
Author:
Publisher
Frontiers Media SA
Subject
General Medicine
Reference10 articles.
1. Gene Editing and Genotoxicity: Targeting the Off-Targets;Blattner;Front. Genome Ed.,2020
2. A Case of Two Adult Brothers with Wiskott-Aldrich Syndrome, One Treated with Gene Therapy and One with HLA-Identical Hematopoietic Stem Cell Transplantation;Consiglieri;J. Clin. Immunol.,2022
3. CRISPR-Cas9 Gene Editing for Sickle Cell Disease and β-Thalassemia. Reply;Frangoul;N. Engl. J. Med.,2021
4. CRISPR-Cas9 In Vivo Gene Editing for Transthyretin Amyloidosis;Gillmore;N. Engl. J. Med.,2021
5. A New Class of Medicines through DNA Editing;Porteus;N. Engl. J. Med.,2019
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1. Update on advances in cystic fibrosis towards a cure and implications for primary care clinicians;Current Problems in Pediatric and Adolescent Health Care;2024-06
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