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BMJ Publishing Group, Journal of Medical Genetics, 1(51), p. 61-67, 2013

DOI: 10.1136/jmedgenet-2013-101938

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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

Journal article published in 2014 by Alexandros Onoufriadis, Amelia Shoemark, Mustafa M. Munye, Chela T. James, Miriam Schmidts, Mitali Patel, Elisabeth M. Rosser, Chiara Bacchelli, Philip L. Beales, Peter J. Scambler, Stephen L. Hart, Jeannette E. Danke-Roelse, John J. Sloper, Sarah Hull, Claire Hogg and other authors.
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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