Article info
Developmental defects
Original article
The kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypes
- Correspondence to Dr Aoife Waters, Birth Defects Research Centre, Institute of Child Health/Great Ormond Street Hospital for Children, London WC1N 1EH, UK; aoife.waters{at}ucl.ac.uk
Citation
The kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypes
Publication history
- Received July 31, 2014
- Revised November 26, 2014
- Accepted November 27, 2014
- First published January 6, 2015.
Online issue publication
February 18, 2015
Article Versions
- Previous version (6 January 2015).
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Supplementary Data
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Files in this Data Supplement:
- Data supplement 1 - Online supplement
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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 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/