Gaucher disease (GD) is an inborn error of metabolism caused by mutations in the gene (GBA) coding for glucocerebrosidase (GCase), inherited in an autosomal recessive pattern. GD patients have up to 9% risk of developing PD.

Parkinson disease in Gaucher disease

Carecchio, Miryam
2017

Abstract

Gaucher disease (GD) is an inborn error of metabolism caused by mutations in the gene (GBA) coding for glucocerebrosidase (GCase), inherited in an autosomal recessive pattern. GD patients have up to 9% risk of developing PD.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11577/3313768
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