Brain sphingolipid metabolism is closely involved in Gaucher disease
Disruption of sphingolipid metabolism led to neurodegeneration in animal models, revealing a new molecular path to Gaucher’s disease.
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Childhood condition poses risk for Parkinson’s disease later in life
In recent years, defects in the glucocerebrosidase (GBA) gene have been identified as significant risk factors for Parkinson’s disease and deficiencies in this gene also
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