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Article

Comprehensive assessment of PINK1 variants in Parkinson's disease.

Neurobiology of aging - 1 Jul 2020

Krohn Lynne, Grenn Francis P, Makarious Mary B, Kim Jonggeol Jeffrey, Bandres-Ciga Sara, Roosen Dorien A, Gan-Or Ziv, Nalls Mike A, Singleton Andrew B, Blauwendraat Cornelis

Abstract excerpt

Multiple genes have been associated with monogenic Parkinson's disease and Parkinsonism syndromes. Mutations in PINK1 (PARK6) have been shown to result in autosomal recessive early-onset Parkinson's disease. In the past decade, several studies have suggested that carrying a single heterozygous PINK1 mutation is associated with increased risk for Parkinson's disease. Here, we comprehensively assess the role of...

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Identifiers

PMID: 32249012
DOI: 10.1016/j.neurobiolaging.2020.03.003
PMCID: PMC7236133

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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