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Publication Detail
Familial childhood-onset progressive cerebellar syndrome associated with the ATP1A3 mutation.
  • Publication Type:
    Journal article
  • Publication Sub Type:
    Article
  • Authors:
    Jaffer F, Fawcett K, Sims D, Heger A, Houlden H, Hanna MG, Kingston H, Sisodiya SM
  • Publication date:
    04/2017
  • Pagination:
    e145
  • Journal:
    Neurology. Genetics
  • Volume:
    3
  • Issue:
    2
  • Medium:
    Electronic-eCollection
  • Language:
    eng
  • Addresses:
    Department of Neurosciences (F.J.), King's College Hospital, London; MRC Centre for Neuromuscular Diseases and Department of Molecular Neuroscience (F.J., H.H., M.G.H.), UCL Institute of Neurology; MRC Computational Genomics Analysis and Training Programme (K.F., D.S., A.H.), University of Oxford; Central Manchester University Hospitals (H.K.); and NIHR UCLH Biomedical Research Centre (S.M.S.), Department of Clinical and Experimental Epilepsy, UCL Institute of Neurology, Queen Square, UK.
Abstract
No abstract found
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Department of Neuromuscular Diseases
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Department of Neuromuscular Diseases
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Faculty of Brain Sciences
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Clinical & Experimental Epilepsy
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