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- W2074873709 abstract "Gene therapy offers an attractive option to the most severe forms of primary immunodeficiency diseases. Identification of disease-associated genes as well as advances in the technology of gene transfer into hematopoietic progenitor cells have set the basis for the first clinical trials. Settings characterized by the potential for a selective advantage provided to transduced cells are the first diseases to target. The recent example of successful treatment of severe combined immunodeficiency-X1 (gammac deficiency) illustrates this potential." @default.
- W2074873709 created "2016-06-24" @default.
- W2074873709 creator A5029004287 @default.
- W2074873709 date "2000-12-01" @default.
- W2074873709 modified "2023-09-26" @default.
- W2074873709 title "Gene therapy of lymphoid primary immunodeficiencies" @default.
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- W2074873709 doi "https://doi.org/10.1097/00008480-200012000-00008" @default.
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