Abstract
The authors describe an efficient method for generating large deletions (>200 nts) of precise length using the PCR-based method of gene splicing by overlap extension (1). This method is technically simple and less time consuming than conventional loop-out mutagenesis techniques requiring preparation of a single-stranded DNA template. © 1995, Humana Press Inc. All rights reserved.
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APA
Senanayake, S. D., & Brian, D. A. (1995). Precise large deletions by the PCR-based overlap extension method. Molecular Biotechnology, 4(1), 13–15. https://doi.org/10.1007/BF02907467
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