Article info

Original article
IFT81, encoding an IFT-B core protein, as a very rare cause of a ciliopathy phenotype

Authors

  1. 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
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Citation

Perrault I, Halbritter J, Porath JD, et al
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

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