CRISPR Genomic Cure Market is driven by gene editing innovations
CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) technology utilizes a specialized protein called Cas9 to target and cut specific strands of DNA. This allows for problematic DNA code to be corrected, which has immense medical potential to cure genetic diseases. CRISPR can target any DNA sequence and has already been used to successfully cure genetic conditions in animal models.
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