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Gene therapy breakthrough offers hope for severe Dravet syndrome casesBy Dr. Liji Thomas, MD Researchers successfully use an adeno-associated viral vector to restore brain function in a mouse ...
Michigan Medicine researchers have developed a SCN1B gene therapy that restores brain function and survival in mice with ...
Recent research takes aim at the a variant in gene SCN1B, which causes a severe form of developmental epileptic encephalopathy.
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