Abstract
CRISPR/cas9 was widely used in medical study because it is fast, cheap, accurate, and efficient in knockout, knock-in, activation, interference and other editing functions. It has gained attention for precise and effect DNA pieces targeting and editing in different kind model systems, including rat, rabbit, and human cells. The paper will going to investigating how Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) is used to solve human disease. Most of the DNA mutation linked to a hereditary illness can be edited using CRISPR and CRISPR-associated protein 9 technology. The following articles will not only talk about disease associated with gene mutations, but also solve disease by changing DNA sequences and removing allergy factor form food. To explain several of the above approaches, a few examples have been selected for this article, including Alzheimer's disease, Hemophilia, Tyrosine, Beta thalassemia, Parkinson's disease, Hepatocellular carcinoma, and Beta Lactoglobulin.
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