Article info
A difficult case
CAPN1 mutations broadening the hereditary spastic paraplegia/spinocerebellar ataxia phenotype
- Correspondence to Dr Jeffrey Lambe, Department of Neurology, St James’s Hospital, Dublin 8, Ireland; jeffrey.lambe{at}ucdconnect.ie
Citation
CAPN1 mutations broadening the hereditary spastic paraplegia/spinocerebellar ataxia phenotype
Publication history
- Accepted March 14, 2018
- First published April 20, 2018.
Online issue publication
January 18, 2019
Article Versions
- Previous version (17 September 2018).
- 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
© Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted.