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Original article
IFT81, encoding an IFT-B core protein, as a very rare cause of a ciliopathy phenotype
- Correspondence to Professor Friedhelm Hildebrandt, Professor of Pediatrics, Harvard Medical School, Director, Division of Nephrology, Investigator, Howard Hughes Medical Institute, Boston Children's Hospital, 300 Longwood Avenue, Boston, MA 02115, USA; friedhelm.hildebrandt{at}childrens.harvard.edu or Dr Jean-Michel Rozet, Director of Research, Head, Laboratory of Genetics in Ophthalmology, INSERM UMR1163, Imagine Institute of Genetic Diseases, 24 boulevard du Montparnasse, 75015 Paris, France; Jean-michel.rozet{at}inserm.fr
Citation
IFT81, encoding an IFT-B core protein, as a very rare cause of a ciliopathy phenotype
Publication history
- Received October 27, 2014
- Revised June 7, 2015
- Accepted June 15, 2015
- First published August 14, 2015.
Online issue publication
September 22, 2015
Supplementary Data
This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.
- Data supplement 1 - Online supplement
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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 terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/