Article info
PDFPhenotypes
Short report
Novel asymptomatic CNS findings in patients with ACVR1/ALK2 mutations causing fibrodysplasia ossificans progressiva
- Correspondence to Dr Mariasavina Severino, Neuroradiology Unit, Istituto Giannina Gaslini, via Gaslini 5, Genoa 16147, Italy; mariasavinaseverino{at}gaslini.org
Citation
Novel asymptomatic CNS findings in patients with ACVR1/ALK2 mutations causing fibrodysplasia ossificans progressiva
Publication history
- Received June 4, 2016
- Revised July 22, 2016
- Accepted August 8, 2016
- First published August 26, 2016.
Online issue publication
November 23, 2016
Article Versions
- Previous version (23 November 2016).
- 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://www.bmj.com/company/products-services/rights-and-licensing/