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Understanding KCNQ Ion Channels and Related Genetic Disorders

This article explores the KCNQ family of ion channels, specifically KCNQ1, KCNQ2, and KCNQ3. It delves into their roles in cellular physiology and their involvement in various genetic disorders. The piece also highlights the mechanisms by which mutations in these genes can lead to pathologies such as Long QT syndrome and neurological disorders. We provide insights into ongoing research and potential therapeutic approaches targeting these channels, contributing to the advancement of precision medicine for affected patients.

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Understanding KCNQ Ion Channels and Related Genetic Disorders

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