Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort
Mov Disord (in press)
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A Novel Nonsense Variant in GRM1 Causes Autosomal Recessive Spinocerebellar Ataxia 13 in a Consanguineous Pakistani Family
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Epigenome-wide association study of human frontal cortex identifies differential methylation in Lewy body pathology
Nat Commun, 13 (1), 4932
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