Pathological mechanisms of motor dysfunction in familial Danish dementia: insights from a knock-in rat model

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Abstract
Familial Danish Dementia (FDD) is a rare autosomal dominant neurodegenerative disorder caused by a mutation in the integral membrane protein 2B (ITM2b) gen
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Funding Information
  • Reta Lila Weston Institute of Neurological Studies
  • NIH (AG033007)
  • NIH (NS104386)