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Paraoxonase gene mutations in amyotrophic lateral sclerosis.

Authors :
Ticozzi, Nicola
LeClerc, Ashley Lyn
Keagle, Pamela J.
Glass, Jonathan D.
Wills, Anne-Marie
van Blitterswijk, Marka
Bosco, Daryl A.
Rodriguez-Leyva, Ildefonso
Gellera, Cinzia
Ratti, Antonia
Taroni, Franco
McKenna-Yasek, Diane
Sapp, Peter C.
Silani, Vincenzo
Furlong, Clement E.
Brown, Robert H.
Landers, John E.
Source :
Annals of Neurology. Jul2010, Vol. 68 Issue 1, p102-107. 6p.
Publication Year :
2010

Abstract

Three clustered, homologous paraoxonase genes ( PON1, PON2, and PON3) have roles in preventing lipid oxidation and detoxifying organophosphates. Recent reports describe a genetic association between the PON genes and sporadic amyotrophic lateral sclerosis (ALS). We now report that in genomic DNA from individuals with familial and sporadic ALS, we have identified at least 7 PON gene mutations that are predicted to alter PON function. ANN NEUROL 2010 [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03645134
Volume :
68
Issue :
1
Database :
Academic Search Index
Journal :
Annals of Neurology
Publication Type :
Academic Journal
Accession number :
71236069
Full Text :
https://doi.org/10.1002/ana.21993