Two approaches for correcting single-gene defects are gene therapy such as is discussed in Section 3-5D and the CRISPR–Cas9 system. Explain why the CRISPR–Cas9 approach can potentially provide more complete restoration of normal tissue function than gene therapy.

Human Heredity: Principles and Issues (MindTap Course List)
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Chapter16: Reproductive Technology, Genetic Testing, And Gene Therapy
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Problem 12QP: In selecting target cells to receive a transferred gene in gene therapy, what factors do you think...
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Two approaches for correcting single-gene defects are gene therapy such as is discussed in Section 3-5D and the CRISPR–Cas9 system. Explain why the CRISPR–Cas9 approach can potentially provide more complete restoration of normal tissue function than gene therapy.

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