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

    LanguageEnglish
    Pages2395-2409
    JournalHuman Molecular Genetics
    Volume12
    Issue number18
    Publication statusPublished - 2003

    Cite this

    Khurshid, TS., Moore, J., Page, AB., Darling, J., Atherton, DJ., Van Steensel, MA., ... 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.
    Khurshid, TS ; Moore, Johnny ; Page, AB ; Darling, J ; Atherton, DJ ; Van Steensel, MA ; Munro, CS ; Amith, FJ ; McGrath, JA. / An unusual N-terminal deletion of the laminin {alpha}3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome. In: Human Molecular Genetics. 2003 ; Vol. 12, No. 18. pp. 2395-2409.
    @article{9460a38608ad41b3906089368435f683,
    title = "An unusual N-terminal deletion of the laminin {alpha}3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome",
    author = "TS Khurshid and Johnny Moore and AB Page and J Darling and DJ Atherton and {Van Steensel}, MA and CS Munro and FJ Amith and JA McGrath",
    year = "2003",
    language = "English",
    volume = "12",
    pages = "2395--2409",
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    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, vol. 12, no. 18, pp. 2395-2409.

    An unusual N-terminal deletion of the laminin {alpha}3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome. / Khurshid, TS; Moore, Johnny; Page, AB; Darling, J; Atherton, DJ; Van Steensel, MA; Munro, CS; Amith, FJ; McGrath, JA.

    In: Human Molecular Genetics, Vol. 12, No. 18, 2003, p. 2395-2409.

    Research output: Contribution to journalArticle

    TY - JOUR

    T1 - An unusual N-terminal deletion of the laminin {alpha}3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome

    AU - Khurshid, TS

    AU - Moore, Johnny

    AU - Page, AB

    AU - Darling, J

    AU - Atherton, DJ

    AU - Van Steensel, MA

    AU - Munro, CS

    AU - Amith, FJ

    AU - McGrath, JA

    PY - 2003

    Y1 - 2003

    M3 - Article

    VL - 12

    SP - 2395

    EP - 2409

    JO - Human Molecular Genetics

    T2 - Human Molecular Genetics

    JF - Human Molecular Genetics

    SN - 0964-6906

    IS - 18

    ER -