Article info
Developmental defects
Original article
Mutations in CEP120 cause Joubert syndrome as well as complex ciliopathy phenotypes
- Correspondence to Professor Enza Maria Valente, Section of Neurosciences, Department of Medicine and Surgery, University of Salerno, 84081, Baronissi (SA), Italy; enzamaria.valente{at}outlook.com
Citation
Mutations in CEP120 cause Joubert syndrome as well as complex ciliopathy phenotypes
Publication history
- Received February 10, 2016
- Revised March 16, 2016
- Accepted April 2, 2016
- First published May 6, 2016.
Online issue publication
August 22, 2016
Article Versions
- Previous version (6 May 2016).
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Copyright information
Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ 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/