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CRISPR to the Rescue: Advances in Gene Editing for the FMR1 Gene
Gene-editing using Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) is promising as a potential therapeutic strategy for many genetic disorders. CRISPR-based therapies are already being assessed in clinical trials, and evaluation of this technology in Fragile X syndrome has been pe...
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| Publicat a: | Brain Sci |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
MDPI
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6357057/ https://ncbi.nlm.nih.gov/pubmed/30669625 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/brainsci9010017 |
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