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Defects in the α‐synuclein, leucine‐rich repeat kinase 2, or glucocerebrosidase genes have been regarded as essential contributors to PD. However, genetic variability of these genes with respect to early‐onset PD… Click to show full abstract
Defects in the α‐synuclein, leucine‐rich repeat kinase 2, or glucocerebrosidase genes have been regarded as essential contributors to PD. However, genetic variability of these genes with respect to early‐onset PD remains poorly defined for the Chinese demographic.
Keywords:
early onset;
evaluating role;
snca lrrk2;
lrrk2 gba;
role snca;
gba chinese
Journal Title: Movement Disorders
Year Published: 2020
Link to full text (if available)
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Journal Title: Movement Disorders
Year Published: 2020
Link to full text (if available)
Share on Social Media: Sign Up to like & get
recommendations!