Identification of amyotrophic lateral sclerosis (ALS) associated genes. Post mortem spinal cord grey matter from sporadic and familial ALS patients compared with controls. Attempt to identify mechanisms by which ALS destroys motor neurons.
GPL80:
[Hu6800] Affymetrix Human Full Length HuGeneFL Array
Citation:
Dangond F, Hwang D, Camelo S, Pasinelli P et al. Molecular signature of late-stage human ALS revealed by expression profiling of postmortem spinal cord gray matter. Physiol Genomics 2004 Jan 15;16(2):229-39. PMID: 14645737
