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Original article
A homozygous nonsense CEP250 mutation combined with a heterozygous nonsense C2orf71 mutation is associated with atypical Usher syndrome

Authors

  1. Correspondence to Professor Dror Sharon, Department of Ophthalmology, Hadassah-Hebrew University Medical Center, POB 12000, Jerusalem 91120, Israel; dror.sharon1{at}gmail.com
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Citation

Khateb S, Zelinger L, Mizrahi-Meissonnier L, et al
A homozygous nonsense CEP250 mutation combined with a heterozygous nonsense C2orf71 mutation is associated with atypical Usher syndrome

Publication history

  • Received January 13, 2014
  • Revised March 10, 2014
  • Accepted April 2, 2014
  • First published April 29, 2014.
Online issue publication 
June 13, 2014

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