PMP22 exon 4 deletion causes ER retention of PMP22 and a gain-of-function allele in CMT1E

Authors

David S. Wang, University of Iowa
Xingyao Wu, University of Iowa
Yunhong Bai, University of Iowa
Craig Zaidman, Washington University School of Medicine in St. Louis
Tiffany Grider, University of Iowa
John Kamholz, University of Iowa
James R. Lupski, Baylor College of Medicine
Anne M. Connolly, Washington University School of Medicine in St. Louis
Michael E. Shy, University of Iowa

Journal

Annals of Clinical and Translational Neurology

Publication Date

2017

Volume

4

Inclusive Pages

236-245

Document Type

Open Access Publication

DOI

10.1002/acn3.395

Rights and Permissions

Wang, D. S., Wu, X., Bai, Y., Zaidman, C., Grider, T., Kamholz, J., Lupski, J. R., Connolly, A. M. and Shy, M. E. (2017), PMP22 exon 4 deletion causes ER retention of PMP22 and a gain-of-function allele in CMT1E. Ann Clin Transl Neurol, 4: 236–245. doi:10.1002/acn3.395 Copyright 2017 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

Recommended Citation

Wang, David S.; Wu, Xingyao; Bai, Yunhong; Zaidman, Craig; Grider, Tiffany; Kamholz, John; Lupski, James R.; Connolly, Anne M.; and Shy, Michael E., "PMP22 exon 4 deletion causes ER retention of PMP22 and a gain-of-function allele in CMT1E." Annals of Clinical and Translational Neurology. 4, 236-245. (2017).
https://digitalcommons.wustl.edu/open_access_pubs/5863