Multisystem proteinopathy due to VCP mutations: A review of clinical heterogeneity and genetic diagnosis

Authors

Gerald Pfeffer, University of Calgary
Grace Lee, University of California Irvine Medical Center
Carly S Pontifex, University of Calgary
Roberto D Fanganiello, Université Laval
Allison Peck, Cure VCP Disease, Inc.
Conrad C Weihl, Washington University School of Medicine in St. Louis
Virginia Kimonis, University of California Irvine Medical Center

Journal

Genes (Basel)

Publication Date

5-27-2022

Volume

13

Issue

6

First Page

963

Document Type

Open Access Publication

DOI

10.3390/genes13060963

Rights and Permissions

Pfeffer, G.; Lee, G.; Pontifex, C.S.; Fanganiello, R.D.; Peck, A.; Weihl, C.C.; Kimonis, V. Multisystem Proteinopathy Due to VCP Mutations: A Review of Clinical Heterogeneity and Genetic Diagnosis. Genes 2022, 13, 963. https://doi.org/10.3390/genes13060963 This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Recommended Citation

Pfeffer, Gerald; Lee, Grace; Pontifex, Carly S; Fanganiello, Roberto D; Peck, Allison; Weihl, Conrad C; and Kimonis, Virginia, "Multisystem proteinopathy due to VCP mutations: A review of clinical heterogeneity and genetic diagnosis." Genes (Basel). 13, 6. 963 (2022).
https://digitalcommons.wustl.edu/oa_4/79