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 |
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Pages (from-to) | 1256-1257 |
Number of pages | 2 |
Journal | Nature medicine |
Volume | 9 |
Issue number | 10 |
DOIs | |
State | Published - Oct 2003 |