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    Genome editing using CRISPR/Cas9 to treat hereditary hematological disorders

    The clustered regularly interspaced short palindromic repeats/CRISPR-associated protein 9 (CRISPR/Cas9) system is a versatile and convenient genome-editing tool with prospects in gene therapy. This technique i...

    Yan Chen, Ruiting Wen, Zhigang Yang, Zhanghui Chen in Gene Therapy (2022)