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Original research
Truncating mutations in exons 20 and 21 of OFD1 can cause primary ciliary dyskinesia without associated syndromic symptoms

Authors

  1. Correspondence to Dr Zuzanna Bukowy-Bieryllo, Institute of Human Genetics, Polish Academy of Sciences, Poznan 60-479, Poland; zuzanna.bukowy-bieryllo{at}igcz.poznan.pl
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Citation

Bukowy-Bieryllo Z, Rabiasz A, Dabrowski M, et al
Truncating mutations in exons 20 and 21 of OFD1 can cause primary ciliary dyskinesia without associated syndromic symptoms

Publication history

  • Received December 2, 2018
  • Revised March 25, 2019
  • Accepted June 28, 2019
  • First published July 31, 2019.
Online issue publication 
October 23, 2019

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