Associated Papers
A pathogenic variant in RAB32 causes autosomal dominant Parkinson's disease and activates LRRK2 kinase.
Gustavsson EK et al.
Medrxiv : the Preprint Server for Health Sciences, 2024
38293014 (PubMed )
Supplement: media-1.pdf
ABCA7 loss-of-function variants, expression, and neurologic disease risk.
Allen M et al.
Neurology. Genetics, 2017
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