ITEM METADATA RECORD
Title: Mitochondrial dysfunction in familial amyotrophic lateral sclerosis
Authors: Faes, Liesbeth
Callewaert, Geert # ×
Issue Date: Dec-2011
Publisher: Plenum Press
Series Title: Journal of Bioenergetics and Biomembranes vol:43 issue:6 pages:587-592
Abstract: A growing body of evidence suggests that mitochondrial dysfunctions play a crucial role in the pathogenesis of various neurodegenerative disorders, including amyotrophic lateral sclerosis (ALS), a neurodegenerative disease affecting both upper and lower motor neurons. Although ALS is predominantly a sporadic disease, approximately 10% of cases are familial. The most frequent familial form is caused by mutations in the gene encoding Cu/Zn superoxide dismutase 1 (SOD1). A dominant toxic gain of function of mutant SOD1 has been considered as the cause of the disease and mitochondria are thought to be key players in the pathogenesis. However, the exact nature of the link between mutant SOD1 and mitochondrial dysfunctions remains to be established. Here, we briefly review the evidence for mitochondrial dysfunctions in familial ALS and discuss a possible link between mutant SOD1 and mitochondrial dysfunction.
ISSN: 0145-479X
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Physiology, Kulak (-)
× corresponding author
# (joint) last author

Files in This Item:

There are no files associated with this item.

 


All items in Lirias are protected by copyright, with all rights reserved.

© Web of science