Combined exome and whole-genome sequencing identifies mutations in ARMC4 as a cause of primary ciliary dyskinesia with defects in the outer dynein arm

A. Onoufriadis, A. Shoemark, M.M. Munye, C.T. James, M. Schmidts, M. Patel, E.M. Rosser, C. Bacchelli, P.L. Beales, P.J. Scambler, S.L. Hart, J.E. nke-Roelse, J.J. Sloper, S. Hull, C. Hogg, R.D. Emes, G. Pals, A.T. Moore, E.M.K. Chung, H.M. Mitchison

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)61-67
JournalJournal of Medical Genetics
Volume51
Issue number1
DOIs
Publication statusPublished - 2014

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