Inherited genetic variants have long been recognized as pivotal contributors to the risk and progression of various diseases. These variants, which are passed down from one generation to the next, can influence disease susceptibility, severity, and response to treatment. Recent advances in genomic technologies have provided a deeper understanding of how specific genetic alterations, such as Single Nucleotide Polymorphisms (SNPs), insertions, deletions, and copy number variations, affect the expression of genes involved in disease pathways.
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