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Article

CX3CR1 is a modifying gene of survival and progression in amyotrophic lateral sclerosis.

PloS one - 1 Jan 2014

Lopez-Lopez Alan, Gamez Josep, Syriani Emilio, Morales Miguel, Salvado Maria, Rodríguez Manuel J, Mahy Nicole, Vidal-Taboada Jose M

Abstract excerpt

The objective of this study was to investigate the association of functional variants of the human CX3CR1 gene (Fractalkine receptor) with the risk of Amyotrophic Lateral Sclerosis (ALS), the survival and the progression rate of the disease symptoms in a Spanish ALS cohort. 187 ALS patients (142...

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Share to Aged, 80 and over
Share to Amyotrophic Lateral Sclerosis
Share to CX3C Chemokine Receptor 1

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 24806473
DOI: 10.1371/journal.pone.0096528
PMCID: PMC4013026

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Prepared record publication-24806473-2026-09-05.1. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 5 Sept 2026.

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