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The review highlights the need for further research into targeted therapies, geneticmarkers, and innovative approaches to prevent cognitive decline, ultimately aiming to optimize long-term outcomes for individuals affected by subarachnoid hemorrhage.
In addition to Mendelian disorders, heart disease risk is influenced by several genetic variants making it a polygenic trait. Researchers identified hundreds of geneticmarkers associated with heart disease risk. These conditions are caused by a single gene mutation and manifest early in life.
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