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UCLA researchers develop base editing approach for rare genetic immune disorder

New research indicates the novel gene editing technique base editing could be used as a one-time therapy to restore the production of T cells in patients born with the rare genetic immune disorder CD3 delta severe combined immunodeficiency. This condition, also known as CD3 delta SCID, is caused by a mutation in the CD3 delta gene, which produces a protein by the same name
United States Donald Kohn Nicola Wright Stem Cell Research Broad Stem Cell Research Center David Geffen School Of Medicine
Source: ucla.edu

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