conference paper
An miRNA-based gene therapy approach to target mutated SOD1 in key cell types in amyotrophic lateral sclerosis (ALS)
December 1, 2018
Human Gene Therapy
Type
conference paper
Web of Science ID
WOS:000453707700257
Author(s)
Date Issued
2018-12-01
Publisher
Publisher place
New Rochelle
Published in
Human Gene Therapy
Volume
29
Issue
12
Start page
A80
End page
A80
Editorial or Peer reviewed
REVIEWED
Written at
EPFL
| Event name | Event place | Event date |
Lausanne, SWITZERLAND | Oct 16-19, 2018 | |
Available on Infoscience
January 3, 2019
Use this identifier to reference this record