Zobrazeno 1 - 8
of 8
pro vyhledávání: '"S. t. George Hyslop P."'
Autor:
Orlacchio, Aldo, Kawarai, T., Polidoro, M., Merlo, S., Gallozzi, M., Perri, R., Di Natale, M., Bruni, A., Orlacchio, A., S. t. George Hyslop P., Bernardi, G.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3982::fe416e441804c13f5bd1d260f27b9140
http://hdl.handle.net/11391/9760
http://hdl.handle.net/11391/9760
Autor:
BRUNI A. M., BERNARDI R., COLAO R., RUBINO E., SMIRNE N., FRANGIPANE F., TERNI B., CURCIO S. A. M., MIRABELLI M., CLODOMIRO A., DiLORENZO R., MALETTA R., ANFOSSI M., GALLO M., GERACITANO S., TOMAINO C., MURACA M. G., LEOTTA A., LIO S. G., PINESSI L., RAINERO I., SORBI S., NEE L., MILAN G., PAPPATA' S., ABBAMONDI N., FORLONI G., S.t. GEORGE HYSLOP P., ROGAEVA E., BUGIANI O., GIACCONE G., FONCIN J. F., SPILLANTINI M. G., PUCCIO G. F., POSTIGLIONE, ALFREDO
OBJECTIVE: Large kindreds segregating familial Alzheimer disease (FAD) offer the opportunity of studying clinical variability as observed for presenilin 1 (PSEN1) mutations. Two early-onset FAD (EOFAD) Calabrian families with PSEN1 Met146Leu (ATG/CTG
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3730::4228b3265dc286549d55197da4f666cb
http://hdl.handle.net/11588/366421
http://hdl.handle.net/11588/366421