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  • K. Kinghorn, Sebastian Grönke, +8 authors L. Partridge
  • Medicine, Biology
  • The Journal of Neuroscience
  • 2016 (First Publication: 16 November 2016)
  • Glucocerebrosidase (GBA1) mutations are associated with Gaucher disease (GD), an autosomal recessive disorder caused by functional deficiency of glucocerebrosidase (GBA), a lysosomal enzyme thatExpand