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 journalArticle

67 Citations (Scopus)
Original languageEnglish
Pages (from-to)2218-2223
JournalInvestigative Ophthalmology and Visual Science
Volume45
Issue number7
DOIs
Publication statusPublished - 2004

Cite this

Yamada, K., Chan, W. M., Andrews, C., Bosley, T. M., Sener, E. C., Zwaan, J. T., Mullaney, P. B., Ozturk, B. T., Akarsu, A. N., Sabol, L. J., Demer, J. L., Sullivan, T. J., Gottlob, I., Roggenkaemper, P., Mackey, D., De Uzcategui, C. E., Uzcategui, N., Ben-Zeev, B., Traboulsi, E. I., ... Engle, E. C. (2004). Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3). Investigative Ophthalmology and Visual Science, 45(7), 2218-2223. https://doi.org/10.1167/iovs.03-1413