Etuvetidigene Autotemcel for the Treatment of Wiskott–Aldrich Syndrome

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Summary

Etuvetidigene Autotemcel for the treatment of Wiskott–Aldrich Syndrome was published in the New England Journal of Medicine. The article presents clinical data on this gene therapy approach for the rare immunodeficiency disorder.

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gene therapyrare diseaseimmunodeficiencyautotemcelNEJM publication

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Published by New England Journal of Medicine on September 23, 2026 9:00 AM

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