Article info
PDFNeuromuscular
Short report
Heterozygous D90A-SOD1 mutation in a patient with facial onset sensory motor neuronopathy (FOSMN) syndrome: a bridge to amyotrophic lateral sclerosis
- Correspondence to Dr Giuseppe Lauria, Headache and Neuroalgology Unit & ALS Clinic, IRCCS Foundation, Carlo Besta Neurological Institute, Via Celoria, 11, Milan 20133, Italy; glauria{at}istituto-besta.it
Citation
Heterozygous D90A-SOD1 mutation in a patient with facial onset sensory motor neuronopathy (FOSMN) syndrome: a bridge to amyotrophic lateral sclerosis
Publication history
- Received December 7, 2013
- Revised January 17, 2014
- Accepted January 29, 2014
- First published March 3, 2014.
Online issue publication
August 06, 2014
Article Versions
- Previous version (3 March 2014).
- You are viewing the most recent version of this article.
Request permissions
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Copyright information
Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions