You are here

Article info

Article menu
Download PDFPDF
New loci
Communications
C14ORF179 encoding IFT43 is mutated in Sensenbrenner syndrome

Authors

  1. Correspondence to Dr Heleen H Arts, Department of Human Genetics (855), Radboud University Nijmegen Medical Centre, Geert Grooteplein Zuid 10, 6525 GA, Nijmegen, The Netherlands; h.arts{at}antrg.umcn.nl
View Full Text

Citation

Arts HH, Bongers EMHF, Mans DA, et al
C14ORF179 encoding IFT43 is mutated in Sensenbrenner syndrome
Journal of Medical Genetics 2011;48:390-395.

Publication history

  • Received January 7, 2011
  • Revised January 24, 2011
  • Accepted January 25, 2011
  • First published March 4, 2011.
Online issue publication 
April 27, 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.

Copyright information

© 2011, 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.