February 01, 1996; 46 (2) BRIEF COMMUNICATION
Genetic heterogeneity in Charcot-Marie-Tooth neuropathy type 2
First published February 1, 1996, DOI: https://doi.org/10.1212/WNL.46.2.569
Genetic heterogeneity in Charcot-Marie-Tooth neuropathy type 2
Neurology Feb 1996, 46 (2) 569-571; DOI: 10.1212/WNL.46.2.569
Citation Manager Formats
Make Comment
See Comments

Article Information
vol. 46 no. 2 569-571
PubMed:
Print ISSN:
Online ISSN:
History:
- First Published February 1, 1996.
Copyright & Usage:
Copyright 1996 by the Advanstar Communication Inc.
Author Disclosures
Article usage
Cited By...
Letters: Rapid online correspondence
No comments have been published for this article.
REQUIREMENTS
If you are uploading a letter concerning an article:
You must have updated your disclosures within six months: http://submit.neurology.org
Your co-authors must send a completed Publishing Agreement Form to Neurology Staff (not necessary for the lead/corresponding author as the form below will suffice) before you upload your comment.
If you are responding to a comment that was written about an article you originally authored:
You (and co-authors) do not need to fill out forms or check disclosures as author forms are still valid
and apply to letter.
Submission specifications:
- Submissions must be < 200 words with < 5 references. Reference 1 must be the article on which you are commenting.
- Submissions should not have more than 5 authors. (Exception: original author replies can include all original authors of the article)
- Submit only on articles published within 6 months of issue date.
- Do not be redundant. Read any comments already posted on the article prior to submission.
- Submitted comments are subject to editing and editor review prior to posting.
You May Also be Interested in
Advertisement
Dr. Jeffrey Allen and Dr. Nicholas Purcell
► Watch
Related Articles
- No related articles found.
Alert Me
Recommended articles
-
Articles
Linkage mapping of the gene for Charcot-Marie-Tooth disease type 2 to chromosome 1p (CMT2A) and the clinical features of CMT2AM. Saito, Y. Hayashi, T. Suzuki et al.Neurology, December 01, 1997 -
Articles
Familial typical migraineLinkage to chromosome 19p13 and evidence for genetic heterogeneityD. R. Nyholt, R. A. Lea, P. J. Goadsby et al.Neurology, May 01, 1998 -
Articles
Clinical and electrophysiologic features of CMT2A with mutations in the mitofusin 2 geneVictoria H. Lawson, Brad V. Graham, Kevin M. Flanigan et al.Neurology, July 25, 2005 -
Articles
Charcot-Marie-Tooth disease type 2 associated with mutation of the myelin protein zero geneM. G. Marrosu, S. Vaccargiu, G. Marrosu et al.Neurology, May 01, 1998