Advancements in CRISPR-Cas9 for Genetic Disorders
Keywords:
CRISPR-Cas9, genetic disorders, gene editing, cystic fibrosis, muscular dystrophyAbstract
This article reviews the latest advancements in CRISPR-Cas9 technology for the treatment of genetic disorders. We assess its application in gene editing for conditions like cystic fibrosis and muscular dystrophy. The precision and efficiency of CRISPR-Cas9 have revolutionized the field, offering potential cures for previously untreatable diseases. Despite ethical concerns and technical challenges, ongoing research continues to advance its clinical applications. This review provides insights into current breakthroughs and future directions for CRISPR-Cas9 in medical science.
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