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Huntington disease Huntington disease is an inherited neurodegenerative disorder caused by expansion of CAG repeats in the Huntingtin ( HTT ) gene [60]

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(3) It inhibits apoptotic markers such as caspase-3 and increases anti-apoptotic factors such as Bcl2 in ischemia [229,230,232]

References 1.Ludwig J., Viggiano T.R., McGill D.B., Oh B.J