Article info
PDFGenotype-phenotype correlations
Original article
A CASQ1 founder mutation in three Italian families with protein aggregate myopathy and hyperCKaemia
- Correspondence to Dr Marina Mora, Muscle Cell Biology Lab, Neuromuscular Diseases and Neuroimmunology Unit, Neurological Institute ‘C Besta’, Via Temolo 4, Milano 20126, Italy; mmora{at}istituto-besta.it and Dr Claudia Di Blasi, Neuromuscular Diseases and Neuroimmunology Unit, Foundation IRCCS, Neurological Institute C Besta, Milano, Italy; cladibl@gmail.com
Citation
A CASQ1 founder mutation in three Italian families with protein aggregate myopathy and hyperCKaemia
Publication history
- Received November 6, 2014
- Revised June 13, 2015
- Accepted June 16, 2015
- First published July 1, 2015.
Online issue publication
August 21, 2017
Article Versions
- Previous version (21 August 2017).
- Previous version (21 August 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
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