Insufficient evidence for pathogenicity of SNCA His50Gln (H50Q) in Parkinson's disease
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DOI: 10.1016/j.neurobiolaging.2017.12.012
Abstract: SNCA missense mutations are a rare cause of autosomal dominant Parkinson's disease (PD). To date, 6 missense mutations in SNCA have been nominated as causal. Here, we assess the frequency of these 6 mutations in public population… read more here.
Keywords: his50gln; parkinson; pathogenicity; parkinson disease ... See more keywords