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Combined exome and whole-genome sequencing identifies mutations in ARMC4 as a cause of primary ciliary dyskinesia with defects in the outer dynein arm
- Correspondence to Dr Hannah M Mitchison, Molecular Medicine Unit, University College London (UCL) Institute of Child Health, London WC1N 1EH, UK; h.mitchison{at}ucl.ac.uk
Citation
Combined exome and whole-genome sequencing identifies mutations in ARMC4 as a cause of primary ciliary dyskinesia with defects in the outer dynein arm
Publication history
- Received July 19, 2013
- Revised September 18, 2013
- Accepted September 19, 2013
- First published November 7, 2013.
Online issue publication
April 27, 2016
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