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Letter
Hereditary spastic paraplegia: a novel mutation and expansion of the phenotype variability in SPG10
- Correspondence to Prof. Antonio Orlacchio, Laboratorio di Neurogenetica, Centro Europeo di Ricerca sul Cervello (CERC)-Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Santa Lucia, 64 Via del Fosso di Fiorano, Rome 00143, Italy; a.orlacchio{at}hsantalucia.it
Citation
Hereditary spastic paraplegia: a novel mutation and expansion of the phenotype variability in SPG10
Publication history
- Received May 22, 2014
- Revised August 30, 2014
- Accepted September 1, 2014
- First published October 28, 2014.
Online issue publication
April 13, 2016
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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 This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/