Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataract

Tianxiao Zhang, Rui Hau, Wei Xiao, Kathryn Burdon, Shomi Bhattacharya, Jamie Craig, Dandan Shang, Xiuli Zhao, David Mackey, Anthony Moore, Yang Luo, Jinsong Zhang, Xue Zhang

    Research output: Contribution to journalArticle

    76 Citations (Scopus)
    Original languageEnglish
    Pages (from-to)E603-E611
    Number of pages9
    JournalHuman Mutation
    Volume30
    Issue number5
    Publication statusPublished - 2009

    Cite this

    Zhang, T., Hau, R., Xiao, W., Burdon, K., Bhattacharya, S., Craig, J., Shang, D., Zhao, X., Mackey, D., Moore, A., Luo, Y., Zhang, J., & Zhang, X. (2009). Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataract. Human Mutation, 30(5), E603-E611.