The legs at odd angles (Loa) mutation in cytoplasmic dynein ameliorates mitochondrial function in SOD1G93A mouse model for motor neuron disease. (2010)
Attributed to:
Analysis of protein interactions of a cytoplasmic dynein mutant which causes motor neuron death.
funded by
BBSRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1074/jbc.m110.129320
PubMed Identifier: 20382740
Publication URI: http://europepmc.org/abstract/MED/20382740
Type: Journal Article/Review
Volume: 285
Parent Publication: The Journal of biological chemistry
Issue: 24
ISSN: 0021-9258