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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
Authors
Publication date
2018-12-01
Publisher
Published in
Human Gene Therapy
Publisher place
New Rochelle
Volume
29
Issue
12
Start page
A80
End page
A80
Peer reviewed
REVIEWED
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