Mutations in SCO2 are associated with autosomal-dominant high-grade myopia
10.1016/j.ajhg.2013.04.005
Saved in:
Main Authors: | Tran-Viet, K.-N., Powell, C., Barathi, V.A., Klemm, T., Maurer-Stroh, S., Limviphuvadh, V., Soler, V., Ho, C., Yanovitch, T., Schneider, G., Li, Y.-J., Nading, E., Metlapally, R., Saw, S.-M., Goh, L., Rozen, S., Young, T.L. |
---|---|
Other Authors: | SAW SWEE HOCK SCHOOL OF PUBLIC HEALTH |
Format: | Article |
Published: |
2014
|
Online Access: | http://scholarbank.nus.edu.sg/handle/10635/108996 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | National University of Singapore |
Similar Items
-
Study of a US cohort supports the role of ZNF644 and high-grade myopia susceptibility
by: Tran-Viet, K.-N., et al.
Published: (2014) -
CYP1B1, MYOC, and LTBP2 mutations in primary congenital glaucoma patients in the United States
by: Lim, S.-H., et al.
Published: (2014) -
Autosomal Dominant Spinocerebellar Ataxias: An Asian Perspective
by: Tan E.K.
Published: (2018) -
PDGFRB mutation causes autosomal-dominant Penttinen syndrome
by: Aminkeng, F
Published: (2022) -
Progressive myopia or hyperopia can be induced in chicks and reversed by manipulation of the chromaticity of ambient light
by: Foulds, W.S., et al.
Published: (2016)