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Neurogenetics
Review
Genetic neurological channelopathies: molecular genetics and clinical phenotypes

Authors

  1. Correspondence to Professor MG Hanna, MRC Centre for Neuromuscular Diseases, P.O. Box 102, National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UK; m.hanna{at}ucl.ac.uk
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Citation

Spillane J, Kullmann DM, Hanna MG
Genetic neurological channelopathies: molecular genetics and clinical phenotypes
Journal of Neurology, Neurosurgery & Psychiatry 2016;87:37-48.

Publication history

  • Received May 11, 2015
  • Revised August 16, 2015
  • Accepted September 13, 2015
  • First published November 11, 2015.
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://www.bmj.com/company/products-services/rights-and-licensing/ 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/