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  4. Gene therapy against amyotrophic lateral sclerosis: a bicistronic AAV vector for RNAi against mutated SOD1
 
conference paper

Gene therapy against amyotrophic lateral sclerosis: a bicistronic AAV vector for RNAi against mutated SOD1

Valdes, P.
•
Colin, P.  
•
Gaudry, J. P.
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December 1, 2022
Human Gene Therapy
29th Annual Congress of the European-Society-of-Gene-and-Cell-Therapy (ESCGT)
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Type
conference paper
Web of Science ID

WOS:000899950600277

Author(s)
Valdes, P.
Colin, P.  
Gaudry, J. P.
Aebi, A.
Schneider, B. L.
Date Issued

2022-12-01

Publisher

MARY ANN LIEBERT, INC

Publisher place

New Rochelle

Published in
Human Gene Therapy
Volume

33

Issue

23-24

Start page

A89

End page

A89

Subjects

Biotechnology & Applied Microbiology

•

Genetics & Heredity

•

Medicine, Research & Experimental

•

Research & Experimental Medicine

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
PTBTG  
Event nameEvent placeEvent date
29th Annual Congress of the European-Society-of-Gene-and-Cell-Therapy (ESCGT)

Edinburgh, SCOTLAND

Oct 11-14, 2022

Available on Infoscience
January 30, 2023
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/194364
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