The mutational spectrum of holoprosencephaly-associated changes within the SHH gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis (Q37411003)

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scientific article published on October 2009
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The mutational spectrum of holoprosencephaly-associated changes within the SHH gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis
scientific article published on October 2009

    Statements

    The mutational spectrum of holoprosencephaly-associated changes within the SHH gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis (English)
    Erich Roessler
    Kenia B El-Jaick
    Christèle Dubourg
    Jorge I Vélez
    Benjamin D Solomon
    Daniel E Pineda-Alvarez
    Nan Zhou
    Maia Ouspenskaia
    Aimée Paulussen
    Hubert J Smeets
    Ute Hehr
    Claude Bendavid
    Sherri Bale
    Sylvie Odent
    Véronique David
    1 October 2009
    E921-35

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