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Promising new gene therapies for sickle cell are out of reach in countries where they re needed most

Promising new gene therapies for sickle cell are out of reach in countries where they re needed most
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Sickle cell breakthrough

The first therapy based on gene editing technology Crispr-Cas9 for sickle cell disease and thalassaemia has been approved in UK. The potential for India is revolutionary however, cost is a huge deterrent currently

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