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Article

Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study.

The Lancet. Neurology - 1 Oct 2010

Laaksovirta Hannu, Peuralinna Terhi, Schymick Jennifer C, Scholz Sonja W, Lai Shaoi-Lin, Myllykangas Liisa, Sulkava Raimo, Jansson Lilja, Hernandez Dena G, Gibbs J Raphael, Nalls Michael A, Heckerman David, Tienari Pentti J, Traynor Bryan J

Abstract excerpt

BACKGROUND: The genetic cause of amyotrophic lateral sclerosis (ALS) is not well understood. Finland is a well suited location for a genome-wide association study of ALS because the incidence of the disease is one of the highest in the world, and because the genetic homogeneity of the Finnish pop...

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Identifiers

PMID: 20801718
DOI: 10.1016/S1474-4422(10)70184-8
PMCID: PMC2965392

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SOD1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20801718-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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