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Exome sequencing in Asian populations identifies low-frequency and rare coding variation influencing Parkinson’s disease risk
Exome sequencing in Asian populations identifies low-frequency and rare coding variation influencing Parkinson’s disease risk
Genetic-based diagnostics of Parkinson’s disease and other Parkinsonian syndromes
GBA1 T369M and Parkinson’s disease – Further evidence of a lack of association in the Swedish population
LRRK2 rare-variant per-domain genetic burden in Parkinson’s Disease.

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+1-514-398-5845
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+1-514-398-5845
ziv.gan-or@mcgill.ca

1033 Pine Avenue West Ludmer Pavilion, room 312, Montreal, QC, H3A 1A1