An unusual N-terminal deletion of the laminin {alpha}3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome

TS Khurshid, Johnny Moore, AB Page, J Darling, DJ Atherton, MA Van Steensel, CS Munro, FJ Amith, JA McGrath

    Research output: Contribution to journalArticle

    Original languageEnglish
    Pages (from-to)2395-2409
    JournalHuman Molecular Genetics
    Volume12
    Issue number18
    Publication statusPublished - 2003

    Cite this

    Khurshid, TS., Moore, J., Page, AB., Darling, J., Atherton, DJ., Van Steensel, MA., Munro, CS., Amith, FJ., & McGrath, JA. (2003). An unusual N-terminal deletion of the laminin {alpha}3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome. Human Molecular Genetics, 12(18), 2395-2409.