conference paper
A miRNA-Based Gene Therapy Approach to Target Mutated SOD1 in Key Cell Types in Amyotrophic Lateral Sclerosis {ALS}
May 1, 2018
Molecular Therapy
Type
conference paper
Web of Science ID
WOS:000435342203124
Author(s)
Date Issued
2018-05-01
Publisher
Publisher place
Cambridge
Published in
Molecular Therapy
Volume
26
Issue
5
Start page
263
End page
263
Editorial or Peer reviewed
REVIEWED
Written at
EPFL
EPFL units
| Event name | Event place | Event date |
Chicago, IL | May 16-19, 2018 | |
Available on Infoscience
December 13, 2018
Use this identifier to reference this record