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Three prevalent mutations in a patient with phenylalanine hydroxylase deficiency: implications for diagnosis and genetic counselling.
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    Citation

    Guldberg P, Levy HL, Henriksen KF, et al
    Three prevalent mutations in a patient with phenylalanine hydroxylase deficiency: implications for diagnosis and genetic counselling.

    Publication history

    • First published February 1, 1996.
    Online issue publication 
    February 01, 1996

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