After A Life Of Painful Sickle Cell Disease, A Patient Hopes Gene-Editing Can Help

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After A Life Of Painful Sickle Cell Disease, A Patient Hopes Gene-Editing Can Help
She's the first patient with a genetic disorder to be treated with the powerful gene-editing technique CRISPR. The treatment has wrapped up, and now she's waiting to see if it brings relief.

Source:  From NPR.org on October 11th 2019.

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Universidad Autonoma de Nuevo Leon, Hematology Service, Hospital Universitario Monterrey, México
E-Mail : dgomezalmaguer@gmail.com

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