Abstract
Amyotrophic lateral sclerosis has not responded well in clinical trials to what initially seemed a promising therapy-the administration of neuronal growth and survival factors. Now, a gene therapy-based approach in mice revives hope that proper delivery of such factors can slow the disease's course.
| Original language | English |
|---|---|
| Pages (from-to) | 1256-1257 |
| Number of pages | 2 |
| Journal | Nature medicine |
| Volume | 9 |
| Issue number | 10 |
| DOIs | |
| State | Published - Oct 2003 |