The novel human p.I587V variant in the ZNF644 gene is unlikely to be the pathogenic cause of dominantly inherited high myopia in a Chinese patient

Emily Jamieson, Douglas H. Lester

    Research output: Contribution to journalLetterpeer-review

    4 Citations (Scopus)
    Original languageEnglish
    Pages (from-to)6728
    Number of pages1
    JournalInvestigative Ophthalmology & Visual Science
    Volume53
    Issue number10
    DOIs
    Publication statusPublished - Sep 2012

    Keywords

    • Ophthalmology
    • Mutations
    • Retinal degeneration

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