Journal Article

Genetics of sporadic amyotrophic lateral sclerosis

J.C. Schymick, K. Talbot and B.J. Traynor

in Human Molecular Genetics

Volume 16, issue R2, pages R233-R242
Published in print October 2007 | ISSN: 0964-6906
Published online October 2007 | e-ISSN: 1460-2083 | DOI:
Genetics of sporadic amyotrophic lateral sclerosis

Show Summary Details


Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized clinically by rapidly progressive paralysis leading ultimately to death from respiratory failure. There is substantial evidence suggesting that ALS is a heritable disease, and a number of genes have been identified as being causative in familial ALS. In contrast, the genetics of the much commoner sporadic form of the disease is poorly understood and no single gene has been definitively shown to increase the risk of developing ALS. In this review, we discuss the genetic evidence for each candidate gene that has been putatively associated with increased risk of sporadic ALS. We also review whole genome association studies of ALS and discuss the potential of this methodology for identifying genes relevant to motor neuron degeneration.

Journal Article.  6457 words. 

Subjects: Genetics and Genomics

Full text: subscription required

How to subscribe Recommend to my Librarian

Users without a subscription are not able to see the full content. Please, subscribe or login to access all content.