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Article

Identification of VPS35 mutations replicated in French families with Parkinson disease.

Neurology - 1 May 2012

Lesage S, Condroyer C, Klebe S, Honoré A, Tison F, Brefel-Courbon C, Dürr A, Brice A

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 22517097
DOI: 10.1212/WNL.0b013e318253d5f2

Genes

VPS35

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

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Identification of VPS35 mutations replicated in French families with Parkinson disease.PMID 22517097Read ↗

VPS35 Mutations in Parkinson DiseaseSemantic proximity Read ↗

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

A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants.Semantic proximity Read ↗

The Role of VPS35 in the Pathobiology of Parkinson’s DiseaseSemantic proximity Read ↗

VPS35 mutations in Parkinson disease.Semantic proximity Read ↗

Deciphering the role of VPS35 in Parkinson's diseaseSemantic proximity Read ↗

A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease.Semantic proximity Read ↗

Frequency of the D620N mutation in VPS35 in Parkinson disease.Semantic proximity Read ↗

Contribution of VPS35 genetic variability to LBD in the Flanders-Belgian population.Semantic proximity Read ↗

Genetic and Phenotypic Basis of Autosomal Dominant Parkinson's Disease in a Large Multi-Center CohortSemantic proximity Read ↗

VPS13C-Another Hint at Mitochondrial Dysfunction in Familial Parkinson's Disease.Semantic proximity Read ↗

Update on genetics of parkinsonism.Semantic proximity Read ↗

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