CRISPR Medicine News, 6 August 2020 | CRISPR corrects FOXP3 in rare childhood disease - CRISPR Medicine

CRISPR corrects rare childhood disease

Rosa Bacchetta and colleagues from Stanford University have demonstrated a smart CRISPR gene editing strategy as a feasible therapy for a rare, life-threatening paediatric autoimmune disease. Read more about the approach to treat IPEX (immune dysregulation, polyendocrinopathy, enteropathy, X-linked) syndrome by inserting the FOXP3 gene at exactly the right spot in the genome in our interview with Bacchetta.

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