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RSS FeedsThe deletion of mutant SOD1 via CRISPR/Cas9/sgRNA prolongs survival in an amyotrophic lateral sclerosis mouse model (Gene Therapy)

 
 

9 december 2019 21:00:58

 
The deletion of mutant SOD1 via CRISPR/Cas9/sgRNA prolongs survival in an amyotrophic lateral sclerosis mouse model (Gene Therapy)
 




 
298 viewsCategory: Genetics, Medicine
 
AAV shedding after intracoronary delivery: just a safety concern? (Gene Therapy)
An engineered serum albumin-binding AAV9 capsid achieves improved liver transduction after intravenous delivery in mice (Gene Therapy)
 
 
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