| Literature DB >> 10371543 |
C Hayward1, S Colville, R J Swingler, D J Brock.
Abstract
We analyzed genomic DNA from ALS patients for mutations in the apurinic/apyrimidinic endonuclease (APEX nuclease) gene. We identified three rare polymorphisms in the untranslated region of the gene and one common two-allele polymorphism (D148E). The allelic frequency D148E was significantly different in sporadic ALS patients compared with controls. A conserved amino acid change and a 4-base pair deletion were also identified in sporadic ALS patients. These data suggest that APEX nuclease may contribute to the etiology of ALS.Entities:
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Year: 1999 PMID: 10371543 DOI: 10.1212/wnl.52.9.1899
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910