Clinical and biochemical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
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3. Autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia: evidence of a phenotypic continuum between dominant and recessive forms;Horvath;Mol Genet Metab,2008
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