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Case Reports in Genetics
Volume 2015, Article ID 239167, 5 pages
http://dx.doi.org/10.1155/2015/239167
Case Report

Rare Manifestation of a c.290 C>T, p.Gly97Glu VCP Mutation

1Department of Neurology, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA
2Department of Pathology, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA
3Department of Neurology, Washington University School of Medicine, St. Louis, MO 63110, USA
4Division of Medical Genetics, Department of Pediatrics, Harbor-UCLA Medical Centre, Los Angeles Biomedical Research Institute, Torrance, CA 90502, USA
5Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, 1501 NW 10 Avenue, Miami, FL 33136, USA

Received 27 January 2015; Accepted 12 March 2015

Academic Editor: Patrick Morrison

Copyright © 2015 Nivedita U. Jerath et al. 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.

How to Cite this Article

Nivedita U. Jerath, Cameron D. Crockett, Steven A. Moore, et al., “Rare Manifestation of a c.290 C>T, p.Gly97Glu VCP Mutation,” Case Reports in Genetics, vol. 2015, Article ID 239167, 5 pages, 2015. https://doi.org/10.1155/2015/239167.