Article info

Download PDFPDF
Original article
Eight further individuals with intellectual disability and epilepsy carrying bi-allelic CNTNAP2 aberrations allow delineation of the mutational and phenotypic spectrum

Authors

  1. Correspondence to Dr Christiane Zweier, Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Schwabachanlage 10, Erlangen 91054, Germany; christiane.zweier{at}uk-erlangen.de
View Full Text

Citation

Smogavec M, Cleall A, Hoyer J, et al
Eight further individuals with intellectual disability and epilepsy carrying bi-allelic CNTNAP2 aberrations allow delineation of the mutational and phenotypic spectrum

Publication history

  • Received March 3, 2016
  • Revised May 20, 2016
  • Accepted June 25, 2016
  • First published July 20, 2016.
Online issue publication 
November 23, 2016

Article Versions

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.