Table of Contents
Journal of Neurodegenerative Diseases
Volume 2013 (2013), Article ID 495873, 5 pages
http://dx.doi.org/10.1155/2013/495873
Clinical Study

The MFN2 V705I Variant Is Not a Disease-Causing Mutation: A Segregation Analysis in a CMT2 Family

1Northcott Neuroscience Laboratory, ANZAC Research Institute, Concord, NSW 2139, Australia
2Sydney Medical School, University of Sydney, Sydney, NSW 2008, Australia
3Molecular Medicine Laboratory, Concord Hospital, Concord, NSW 2139, Australia

Received 25 July 2012; Revised 23 October 2012; Accepted 23 October 2012

Academic Editor: Eng King Tan

Copyright © 2013 Obaid M. Albulym 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

Obaid M. Albulym, Danqing Zhu, Stephen Reddel, Marina Kennerson, and Garth Nicholson, “The MFN2 V705I Variant Is Not a Disease-Causing Mutation: A Segregation Analysis in a CMT2 Family,” Journal of Neurodegenerative Diseases, vol. 2013, Article ID 495873, 5 pages, 2013. doi:10.1155/2013/495873