The CRISPR-Cas9 system is a way of editing genes in order to cure diseases or other genetic defects. It has been used to treat congenital blindness and sickle cell disease, among other things.
However, there are still many areas where this technology is not particularly useful for humans. For example, we have not yet been able to successfully use CRISPR on human embryos on a large scale because it would cause unintended changes in the embryo’s DNA that could lead to birth defects.
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