Yamada, K. Et Al. 2004. Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3). INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE , vol.45, no.7 , 2218-2223.

Yamada, K., Chan, W., Andrews, C., Bosley, T., Sener, E., Zwaan, J., ... Mullaney, P.(2004). Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3). INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE , vol.45, no.7, 2218-2223.

Yamada, K Et Al. "Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3)," INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE , vol.45, no.7, 2218-2223, 2004

Yamada, K Et Al. "Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3)." INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE , vol.45, no.7, pp.2218-2223, 2004

Yamada, K. Et Al. (2004) . "Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3)." INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE , vol.45, no.7, pp.2218-2223.

@article{article, author={K Yamada Et Al. }, title={Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3)}, journal={INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE}, year=2004, pages={2218-2223} }