RPE und Gentherapie
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-031-35055-9_15
Reference78 articles.
1. Sengillo JD, Justus S, Cabral T, Tsang SH. Correction of monogenic and common retinal disorders with gene therapy. Genes (Basel). 2017;8(2).
2. Yanik M, Müller B, Song F, Gall J, Wagner F, Wende W, et al. In vivo genome editing as a potential treatment strategy for inherited retinal dystrophies. Prog Retin Eye Res [Internet]. 2017;56:1–18. https://doi.org/10.1016/j.preteyeres.2016.09.001.
3. Cox DBT, Platt RJ, Zhang F. Therapeutic genome editing: prospects and challenges. Nat Med [Internet]. 2015;21(2):121–31. http://www.nature.com/doifinder/10.1038/nm.3793.
4. Maeder ML, Gersbach CA. Genome-editing technologies for gene and cell therapy. Mol Ther [Internet]. 2016;24(3):430–46. http://linkinghub.elsevier.com/retrieve/pii/S1525001616309613.
5. Simunovic MP, Xue K, Jolly JK, MacLaren RE. Structural and functional recovery following limited iatrogenic macular detachment for retinal gene therapy. JAMA Ophthalmol. 2017;135(3):234–41.
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