Hereditary hyperferritinemia-cataract syndrome: prevalence, lens morphology, spectrum of mutations, and clinical presentations

Jamie Craig, J Clark, J Mcleod, M Kirkland, G Grant, J Elder, M Toohey, L Kowal, H Savoia, C Chen, S Roberts, M Wirth, David Mackey

    Research output: Contribution to journalArticle

    50 Citations (Scopus)
    Original languageEnglish
    Article numberCC
    Pages (from-to)1753-1761
    Number of pages9
    JournalArchives of Ophthalmology
    Volume121
    Issue number12
    Publication statusPublished - 2003

    Cite this

    Craig, J., Clark, J., Mcleod, J., Kirkland, M., Grant, G., Elder, J., Toohey, M., Kowal, L., Savoia, H., Chen, C., Roberts, S., Wirth, M., & Mackey, D. (2003). Hereditary hyperferritinemia-cataract syndrome: prevalence, lens morphology, spectrum of mutations, and clinical presentations. Archives of Ophthalmology, 121(12), 1753-1761. [CC].