Analysis of common and rare <i>VPS13C</i> variants in late-onset Parkinson disease

Uladzislau Rudakou, Jennifer A. Ruskey, Lynne Krohn, Sandra B. Laurent, Dan Spiegelman, Lior Greenbaum, Gilad Yahalom, Alex Désautels, Jacques Montplaisir, Stanley Fahn,

Neurology Genetics · 2020 · 26 citations · 18 references

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Abstract

Our results do not support a role for rare heterozygous or biallelic <i>VPS13C</i> variants in LOPD. Additional genetic replication and functional studies are needed to examine the role of the haplotype identified here associated with reduced risk for PD.

References

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