Article info
PDFGenotype-phenotype correlations
Original article
Delineation of CCDC39/CCDC40 mutation spectrum and associated phenotypes in primary ciliary dyskinesia
- Correspondence to Serge Amselem, Service de génétique et d'embryologie médicales, Hôpital Armand-Trousseau, 26 avenue du Dr Arnorld Netter, 75012 Paris, France; serge.amselem{at}inserm.fr
Citation
Delineation of CCDC39/CCDC40 mutation spectrum and associated phenotypes in primary ciliary dyskinesia
Publication history
- Received March 5, 2012
- Revised April 16, 2012
- Accepted April 18, 2012
- First published June 12, 2012.
Online issue publication
April 27, 2016
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© 2012, 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.