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Therapeutic gene editing strategies using CRISPR-Cas9 for the β-hemoglobinopathies

With advancements in gene editing technologies, our ability to make precise and efficient modifications to the genome is increasing at a remarkable rate, paving the way for scientists and clinicians to uniquely treat a multitude of previously irremediable diseases. CRISPR-Cas9, short for clustered r...

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Detalhes bibliográficos
Publicado no:J Biomed Res
Main Authors: Papizan, James B., Porter, Shaina N., Sharma, Akshay, Pruett-Miller, Shondra M.
Formato: Artigo
Idioma:Inglês
Publicado em: Editorial Department of Journal of Biomedical Research 2021
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8038529/
https://ncbi.nlm.nih.gov/pubmed/33349624
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7555/JBR.34.20200096
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