A novel missense mutation in human TTF-2 (FKHL15) gene associated with congenital hypothyroidism but not athyreosis (Q28118845)

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A novel missense mutation in human TTF-2 (FKHL15) gene associated with congenital hypothyroidism but not athyreosis
scientific journal article

    Statements

    A novel missense mutation in human TTF-2 (FKHL15) gene associated with congenital hypothyroidism but not athyreosis (English)
    I. Baris
    A. E. Arisoy
    A. Smith
    M. Agostini
    C. S. Mitchell
    S. M. Park
    A. M. Halefoglu
    E. Zengin
    V. K. Chatterjee
    E. Battaloglu
    1 October 2006
    4183–4187

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