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Article

Frequency of the D620N mutation in VPS35 in Parkinson disease.

Archives of neurology - 1 Oct 2012

Kumar Kishore R, Weissbach Anne, Heldmann Marcus, Kasten Meike, Tunc Sinem, Sue Carolyn M, Svetel Marina, Kostić Vladimir S, Segura-Aguilar Juan, Ramirez Alfredo, Simon David K, Vieregge Peter, Münte Thomas F, Hagenah Johann, Klein Christine, Lohmann Katja

Abstract excerpt

OBJECTIVE: To evaluate the frequency and clinical spectrum of the recently identified p.D620N mutation in the VPS35 gene in Parkinson disease (PD) in an international sample. DESIGN: Genetic analysis by DNA sequencing and detailed clinical and neuropsychiatric assessment as well as neuroimaging i...

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Source

Identifiers

PMID: 22801713
DOI: 10.1001/archneurol.2011.3367

Genes

VPS35

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-22801713-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

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Frequency of the D620N mutation in VPS35 in Parkinson disease.PMID 22801713Read ↗

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Parkinson's disease-associated pathogenic VPS35 mutation causes complex I deficitsSemantic proximity Read ↗

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