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. Magli; T. De Berardinis; V. Gagliardi; S. Awasthi-Patney; M.C. Vogel; J.F. Rizzo Iii; E.C. Engle

doi:10.1167/iovs.03-1413

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

Centre for Ophthalmology and Visual Science (affiliated with the Lions Eye Institute)

Research output: Contribution to journal › Article › peer-review

81 Citations (Scopus)

Original language	English
Pages (from-to)	2218-2223
Journal	Investigative Ophthalmology and Visual Science
Volume	45
Issue number	7
DOIs	https://doi.org/10.1167/iovs.03-1413
Publication status	Published - 2004

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10.1167/iovs.03-1413

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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

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

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volume = "45",

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Yamada, K, Chan, WM, Andrews, C, Bosley, TM, Sener, EC, Zwaan, JT, Mullaney, PB, Ozturk, BT, Akarsu, AN, Sabol, LJ, Demer, JL, Sullivan, TJ, Gottlob, I, Roggenkaemper, P, Mackey, D, De Uzcategui, CE, Uzcategui, N, Ben-Zeev, B, Traboulsi, EI, Magli, A, De Berardinis, T, Gagliardi, V, Awasthi-Patney, S, Vogel, MC, Rizzo Iii, JF & Engle, EC 2004, 'Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3)', Investigative Ophthalmology and Visual Science, vol. 45, no. 7, pp. 2218-2223. https://doi.org/10.1167/iovs.03-1413

TY - JOUR

T1 - Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3)

AU - Yamada, K.

AU - Chan, W.M.

AU - Andrews, C.

AU - Bosley, T.M.

AU - Sener, E.C.

AU - Zwaan, J.T.

AU - Mullaney, P.B.

AU - Ozturk, B.T.

AU - Akarsu, A.N.

AU - Sabol, L.J.

AU - Demer, J.L.

AU - Sullivan, T.J.

AU - Gottlob, I.

AU - Roggenkaemper, P.

AU - Mackey, David

AU - De Uzcategui, C.E.

AU - Uzcategui, N.

AU - Ben-Zeev, B.

AU - Traboulsi, E.I.

AU - Magli, A.

AU - De Berardinis, T.

AU - Gagliardi, V.

AU - Awasthi-Patney, S.

AU - Vogel, M.C.

AU - Rizzo Iii, J.F.

AU - Engle, E.C.

PY - 2004

Y1 - 2004

U2 - 10.1167/iovs.03-1413

DO - 10.1167/iovs.03-1413

M3 - Article

VL - 45

SP - 2218

EP - 2223

JO - Investigative Ophthalmology & Visual Science (IOVS)

JF - Investigative Ophthalmology & Visual Science (IOVS)

SN - 0146-0404

IS - 7

ER -