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Article

P2RX7 genotype association in severe sepsis identified by a novel Multi-Individual Array for rapid screening and replication of risk SNPs.

Clinica chimica acta; international journal of clinical chemistry - 18 Jan 2012

Geistlinger J, Du W, Groll J, Liu F, Hoegel J, Foehr K J, Pasquarelli A, Schneider E M

Abstract excerpt

BACKGROUND: Functional single nucleotide polymorphisms (SNPs) are relevant to individual therapeutic approaches and may play a role in disease susceptibility. Genome-wide scans, which are now widely applied to detect disease-associated SNPs, provide only limited evidence about SNP associations. Their usefulness as disease markers requires appropriate phenotype analysis and retesting of the gene providing SNP...

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Source

Identifiers

PMID: 21640086
DOI: 10.1016/j.cca.2011.05.023

Genes

MIA

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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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