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Article

Association study between XRCC1 gene polymorphisms and sporadic amyotrophic lateral sclerosis.

Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases - 1 Jan 2010

Coppedè Fabio, Migheli Francesca, Lo Gerfo Annalisa, Fabbrizi Maria Rita, Carlesi Cecilia, Mancuso Michelangelo, Corti Stefania, Mezzina Nicoletta, del Bo Roberto, Comi Giacomo P, Siciliano Gabriele, Migliore Lucia

Abstract excerpt

The aim of the present study was to investigate the possible contribution of three common functional polymorphisms in the DNA repair protein X-ray repair cross-complementing group 1 (XRCC1), namely Arg194Trp (rs1799782), Arg280His (rs25489) and Arg399Gln (rs25487), to sporadic amyotrophic lateral sclerosis (SALS). We genotyped 206 Italian SALS patients and 203 matched controls for XRCC1 Arg194Trp, Arg280His and...

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Share to Aged, 80 and over
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Share to DNA-Binding Proteins
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Source

Identifiers

PMID: 19707910
DOI: 10.3109/17482960903220297

Genes

XRCC1

Provenance

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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