Clinical and biochemical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia (Q57206840)

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Clinical and biochemical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia
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    Clinical and biochemical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia (English)
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    Thomas Opladen
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    Georg Hoffmann
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    Friederike Hörster
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    Anne-Bärbel Hinz
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    Katharina Neidhardt
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    3 September 2010
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    26
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    1
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    157-161
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