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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English | 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 |
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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 (English)
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Maher Kharrat
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Véronique Tardy
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Ridha M'Rad
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Faouzi Maazoul
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Lamia Ben Jemaa
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Mohamed Refaï
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Yves Morel
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Habiba Chaabouni
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1 January 2004
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