DOI:
10.1055/s-00000041
Neuropediatrics
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References
López-Laso E, Ochoa-Sepúlveda JJ, Ochoa-Amor JJ. , et al.
Segawa syndrome due to mutation Q89X in the GCH1 gene: a possible founder effect in Córdoba (southern Spain).
J Neurol 2009;
256 (11) 1816-1824
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