Gene Therapy for Rare Disease is Estimated to Witness High Growth Owing to Rising Prevalence of Rare Diseases
Gene therapy involves the delivery of corrective genes to treat rare diseases caused by missing or defective genes. It has shown great potential in the treatment of inherited disorders like hemophilia, cystic fibrosis, and muscular dystrophy. These therapies aim to either introduce a normal copy of the defective gene or inactivate a mutated gene that is responsible for causing the disease. As...
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