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	161.	MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients: hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved region. [electronic resource] by Vacca, M Filippini, F Budillon, A Rossi, V Della Ragione, F De Bonis, M L Mercadante, G Manzati, E Gualandi, F Bigoni, S Trabanelli, C Pini, G Calzolari, E Ferlini, A Meloni, I Hayek, G Zappella, M Renieri, A D'Urso, M D'Esposito, M Macdonald, F Kerr, A Dhanjal, S Hulten, M Producer: 20020313 In: Brain & development vol. 23 Suppl 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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