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DGNeurologie

, Volume 1, Issue 1, pp 58–59 | Cite as

Mutationen im VSP13D-Gen verursachen eine oftmals frühkindliche spastische Ataxie

  • A. GrünewaldEmail author
Scientific News
  • 19 Downloads

Mutations in VSP13D cause spastic ataxia commonly occurring in infancy

Literatur

  1. 1.
    Rzepnikowska W et al (2017) Yeast and other lower eukaryotic organisms for studies of Vps13 proteins in health and disease. Traffic 18:711–719CrossRefGoogle Scholar
  2. 2.
    Anding AL et al (2018) Vps13D encodes a ubiquitin-binding protein that is required for the regulation of mitochondrial size and clearance. Curr Biol 28:287–295.e6CrossRefGoogle Scholar

Copyright information

© Springer Medizin Verlag GmbH, ein Teil von Springer Nature 2018

Authors and Affiliations

  1. 1.Molecular and Functional Neurobiology Group, Luxembourg Centre for Systems BiomedicineUniversité du LuxembourgEsch-sur-AlzetteLuxemburg
  2. 2.Institute of NeurogeneticsUniversity of LübeckLübeckDeutschland

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