Abstract
Inherited neurological disorders are a diverse group of diseases caused by genetic mutations that affect the nervous system. This article explores genetic approaches used to study inherited neurological disorders, with a focus on the identification of disease-causing mutations, the underlying mechanisms of these diseases, and how genetic research is advancing our understanding of these conditions. The article discusses the role of next-generation sequencing, gene editing, and animal models in uncovering the genetic basis of neurological diseases such as Alzheimer's disease, Parkinson's disease, and Huntington's disease. Additionally, the article highlights potential therapeutic strategies, including gene therapy and personalized medicine, based on genetic insights.
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