Article info
PDFPhenotypes
Original article
Patients with a phenotype consistent with facioscapulohumeral muscular dystrophy display genetic and epigenetic heterogeneity
- Correspondence to Dr Sabrina Sacconi, Centre de référence des maladies neuromusculaires, Archet 1 Hospital, 151 Route de Saint Antoine de Ginestière, 06000 Nice, France; sacconi{at}unice.fr
Citation
Patients with a phenotype consistent with facioscapulohumeral muscular dystrophy display genetic and epigenetic heterogeneity
Publication history
- Received April 4, 2011
- Revised August 29, 2011
- Accepted August 30, 2011
- First published October 7, 2011.
Online issue publication
June 21, 2017
Article Versions
- Previous version (21 June 2017).
- 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
© 2011, 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.