Associated Papers
A PheWAS approach to identify associations of GBA1 variants with comprehensive phenotypes beyond neurological diseases.
Yang J et al.
Npj Parkinson's Disease, 2025
40097465 (PubMed )
Supplement: 41531_2025_901_MOESM1_ESM.xlsx › Supplementary_Table_4
Screening of GBA Mutations in Nigerian Patients with Parkinson's Disease.
Milanowski LM et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2021
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