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Mencarelli, M. et al. (2010). Novel FOXG1 mutations associated with the congenital variant of Rett syndrome. Journal of medical genetics. 47 (1), pp. 49-53. [Online].
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Mencarelli, M. et al. (2010). Novel FOXG1 mutations associated with the congenital variant of Rett syndrome. Journal of medical genetics. 47 (1), pp. 49-53. [Online].