将CRISPR/Cas技术与临床试验相结合:原则,进展和挑战

Piao Yang1, Mohadeseh Khoshandam2,3, Iman Bhia4

  • 1Department of Molecular Genetics, College of Arts and Sciences, The Ohio State University, Columbus OH 43210, USA.

概括

基因编辑CRISPR为治疗遗传疾病,神经疾病和癌症提供了革命性的潜力. 本次审查强调了基于CRISPR的治疗方法的创新治疗设计和效率改进,解决了临床应用中的未来挑战.

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