4.7 Article

Paraoxonase Gene Mutations in Amyotrophic Lateral Sclerosis

期刊

ANNALS OF NEUROLOGY
卷 68, 期 1, 页码 102-107

出版社

WILEY
DOI: 10.1002/ana.21993

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资金

  1. ALS Therapy Alliance
  2. Angel Fund
  3. Pierre L. de Bourgknecht ALS Research Foundation
  4. Al-Athel ALS Research Foundation
  5. ALS Family Charitable Foundation
  6. Packard Center for ALS Research
  7. American Academy of Neurology Foundation/ALS Association
  8. National Institute of Neurological Disorders and Stroke [IRO1NS050557-03]
  9. NIH National Institute of Environmental Health Sciences [RO1ES09883-04A2]
  10. Italian Ministry of Health [ex Art.56, n.533F/N1, RF2007/INN644440]
  11. Peviani family

向作者/读者索取更多资源

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;68:102-107

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