Molecular genetic analysis of Tunisian patients with a classic form of 21-hydroxylase deficiency: identification of four novel mutations and high prevalence of Q318X mutation (Q39133005)

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scientific article published on January 2004
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Molecular genetic analysis of Tunisian patients with a classic form of 21-hydroxylase deficiency: identification of four novel mutations and high prevalence of Q318X mutation
scientific article published on January 2004

    Statements

    Molecular genetic analysis of Tunisian patients with a classic form of 21-hydroxylase deficiency: identification of four novel mutations and high prevalence of Q318X mutation (English)
    Maher Kharrat
    Véronique Tardy
    Ridha M'Rad
    Faouzi Maazoul
    Lamia Ben Jemaa
    Mohamed Refaï
    Yves Morel
    Habiba Chaabouni
    1 January 2004
    368-374

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