Abstract
In this issue of Blood, Hubbard et al provide important proof-of-concept data on the utility of using genome editing to knock-in a wild-type (WT) complementary DNA (cDNA) to functionally correct disease-causing mutations in a gene in primary human T cells.1
Cite
CITATION STYLE
APA
Porteus, M. H. (2016, May 26). Knock-in editing: It functionally corrects! Blood. American Society of Hematology. https://doi.org/10.1182/blood-2016-03-703181
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