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

68 Citations (Scopus)
Original languageUndefined/Unknown
Pages (from-to)61-67
JournalJournal of medical genetics
Issue number1
Publication statusPublished - 2014

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