1. Fabry disease: molecular studies in Italian patients and X inactivation analysis in manifesting carriers. Issue 8 (14th August 2003) Authors: Morrone, A; Cavicchi, C; Bardelli, T; Antuzzi, D; Parini, R; Di Rocco, M; Feriozzi, S; Gabrielli, O; Barone, R; Pistone, G; Spisni, C; Ricci, R; Zammarchi, E Journal: Journal of medical genetics Issue: Volume 40:Issue 8(2003) Page Start: e103 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Mutation identification of Fabry disease in families with other lysosomal storage disorders. (28th December 2012) Authors: Zampetti, A; Fania, L; Antuzzi, D; Giurdanella, F; Gnarra, M; Bertola, F; Lualdi, S; Filocamo, M; Morrone, A; Feliciani, C Journal: Clinical genetics Issue: Volume 84:Number 3(2013:Sep.) Page Start: 281 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗