Yanhua Qi
Department of Ophthalmology
The Second Affiliated Hospital
Haerbin Medical University
Haerbin
China
Name/email consistency: high
- A deletion mutation in the betaA1/A3 crystallin gene ( CRYBA1/A3) is associated with autosomal dominant congenital nuclear cataract in a Chinese family. Qi, Y., Jia, H., Huang, S., Lin, H., Gu, J., Su, H., Zhang, T., Gao, Y., Qu, L., Li, D., Li, Y. Hum. Genet. (2004)
