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Article

Genetic Mutation Analysis of Parkinson's Disease Patients Using Multigene Next-Generation Sequencing Panels.

Molecular diagnosis & therapy - 1 Oct 2016

Gorostidi Ana, Martí-Massó José Félix, Bergareche Alberto, Rodríguez-Oroz Mari Cruz, López de Munain Adolfo, Ruiz-Martínez Javier

Abstract excerpt

BACKGROUND: Parkinson's disease (PD) is the second most common neurodegenerative disorder, affecting millions of people. Genome-wide association studies (GWAS) have found >25 genetic risk factors and at least 15 loci directly associated with PD. Recent advances in new next-generation DNA sequencing technologies, such as the semiconductor-based Ion Torrent platform, make multigene sequencing cheaper, faster, and...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 27294386
DOI: 10.1007/s40291-016-0216-1

Genes

ACMSD
APOE
FBXO7
GIGYF2
PARK7
PINK1
SNCA
UCHL1
VPS35

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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