Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3)

K. Yamada, W.M. Chan, C. Andrews, T.M. Bosley, E.C. Sener, J.T. Zwaan, P.B. Mullaney, B.T. Ozturk, A.N. Akarsu, L.J. Sabol, J.L. Demer, T.J. Sullivan, I. Gottlob, P. Roggenkaemper, David Mackey, C.E. De Uzcategui, N. Uzcategui, B. Ben-Zeev, E.I. Traboulsi, A. MagliT. De Berardinis, V. Gagliardi, S. Awasthi-Patney, M.C. Vogel, J.F. Rizzo Iii, E.C. Engle

Research output: Contribution to journalArticlepeer-review

81 Citations (Scopus)
Original languageEnglish
Pages (from-to)2218-2223
JournalInvestigative Ophthalmology and Visual Science
Issue number7
Publication statusPublished - 2004

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