Viral vectors are essential tools in gene therapy, enabling the delivery of nonmutated genes to correct genetic abnormalities.
Viral vectors play a crucial role in gene therapy due to their ability to deliver nonmutated genes into a patient's genome. By utilizing viruses as carriers of genes (viral vectors), scientists can target specific cells and replace disease-causing genes with functional ones, ultimately correcting genetic abnormalities. Scientists have genetically altered viruses like adenoviruses to safely transport therapeutic human genes and insert them into target cells, paving the way for potential treatments of various genetic diseases.
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