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History
- October 31, 2019.
Article Versions
- Version 1 (July 22, 2019 - 13:37).
- You are viewing Version 2, the most recent version of this article.
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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
Author Information
- Junho Kim1,
- Boxun Zhao1,
- August Yue Huang1,
- Michael B. Miller1,2,3,
- Michael A. Lodato1,2,4,
- Christopher A. Walsh1,2,* and
- Eunjung Alice Lee1,*
- 1Division of Genetics and Genomics, Manton Center for Orphan Disease, Boston Children’s Hospital, Boston, MA, USA; Department of Pediatrics, Harvard Medical School, Boston, MA, USA; and Broad Institute of MIT and Harvard, Cambridge, MA, USA
- 2Howard Hughes Medical Institute, Boston Children’s Hospital, Boston, MA, USA and Department of Neurology, Harvard Medical School, Boston, MA, USA
- 3Department of Pathology, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, USA
- 4Department of Cell, Molecular, and Cancer Biology, University of Massachusetts Medical School, Worcester, MA, USA
- ↵*to whom correspondence should be addressed. E-mail: Christopher.Walsh{at}childrens.harvard.edu or EAlice.Lee{at}childrens.harvard.edu
Posted October 31, 2019.
Evidence that APP gene copy number changes reflect recombinant vector contamination
