Genome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore Chinese
10.1016/j.ophtha.2010.06.016
Saved in:
Main Authors: | Li, Y.-J., Goh, L., Khor, C.-C., Fan, Q., Yu, M., Han, S., Sim, X., Ong, R.T.-H., Wong, T.-Y., Vithana, E.N., Yap, E., Nakanishi, H., Matsuda, F., Ohno-Matsui, K., Yoshimura, N., Seielstad, M., Tai, E.-S., Young, T.L., Saw, S.-M. |
---|---|
Other Authors: | LIFE SCIENCES INSTITUTE |
Format: | Article |
Published: |
2014
|
Online Access: | http://scholarbank.nus.edu.sg/handle/10635/108389 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | National University of Singapore |
Similar Items
-
Genetic variants on chromosome 1q41 influence ocular axial length and high myopia
by: Fan, Q., et al.
Published: (2014) -
Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia
by: Khor, C.C., et al.
Published: (2014) -
Myopia
by: Morgan, I.G., et al.
Published: (2014) -
Myopia-related fundus changes in Singapore adults with high myopia
by: Chang, L., et al.
Published: (2014) -
Genetic variants linked to myopic macular degeneration in persons with high myopia: CREAM Consortium
by: Wong, Y.-L., et al.
Published: (2021)